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Dayang Chem (Hangzhou) Co.,Ltd.

DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe

Homovanillyl alcohol

Cas:2380-78-1

Min.Order:1 Kilogram

FOB Price: $3.0

Type:Lab/Research institutions

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Kono Chem Co.,Ltd

Xi'an Kono Chem Co., Ltd., founded in 2014, is a holding enterprise of Hongkong Pioneer Biotech Group. It is an export-oriented manufacturing enterprise supported by the Ministry of Commerce. Kono Chem is located in Xi'an, Shaanxi Province,

Factory Supply Homovanillyl alcohol CAS 2380-78-1

Cas:2380-78-1

Min.Order:1 Kilogram

FOB Price: $52.0 / 55.0

Type:Other

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Hebei Nengqian Chemical Import and Export Co., LTD

Our Advantage Rich Experience Our products are sold all over Europe,North&South America, Sino-East, Asia and pacific area as well as Africa,we establish long term. Quality service Company cooperates with research institutes. We strictly con

Homovanillyl alcohol CAS 2380-78-1

Cas:2380-78-1

Min.Order:1 Kilogram

FOB Price: $1.0 / 10.0

Type:Trading Company

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Zhuozhou Wenxi import and Export Co., Ltd

WITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et

Manufacturer supply CAS 2380-78-1 with best quality

Cas:2380-78-1

Min.Order:1 Kilogram

FOB Price: $139.0 / 210.0

Type:Trading Company

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Shanghai Upbio Tech Co.,Ltd

1.In No Less 10 years exporting experience. you can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specializ

Benzeneethanol,4-hydroxy-3-methoxy-

Cas:2380-78-1

Min.Order:1 Gram

Negotiable

Type:Lab/Research institutions

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Qingdao Beluga Import and Export Co., LTD

Homovanillyl alcohol CAS:2380-78-1 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic inter

Homovanillyl alcohol CAS:2380-78-1

Cas:2380-78-1

Min.Order:1 Gram

Negotiable

Type:Lab/Research institutions

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Shandong Hanjiang Chemical Co., Ltd.

Hello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai

Benzeneethanol,4-hydroxy-3-methoxy-

Cas:2380-78-1

Min.Order:1 Kilogram

Negotiable

Type:Lab/Research institutions

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Henan Wentao Chemical Product Co., Ltd.

Henan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod

Benzeneethanol,4-hydroxy-3-methoxy-

Cas:2380-78-1

Min.Order:0

Negotiable

Type:Lab/Research institutions

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Hangzhou J&H Chemical Co., Ltd.

J&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia

4-Hydroxy-3-methoxyphenethanol

Cas:2380-78-1

Min.Order:0

Negotiable

Type:Lab/Research institutions

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Zibo Hangyu Biotechnology Development Co., Ltd

Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi

4-(2-hydroxyethyl)-2-methoxyphenol

Cas:2380-78-1

Min.Order:10 Gram

FOB Price: $100.0

Type:Lab/Research institutions

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Henan Tianfu Chemical Co., Ltd.

Our company was built in 2009 with an ISO certificate.In the past 6 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so

TIANFUCHEM--2380-78-1---Homovanillyl alcohol

Cas:2380-78-1

Min.Order:1 Metric Ton

FOB Price: $5000.0

Type:Lab/Research institutions

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EAST CHEMSOURCES LIMITED

factory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B

Homovanillyl alcohol CAS NO.2380-78-1

Cas:2380-78-1

Min.Order:1 Kilogram

FOB Price: $18.0 / 20.0

Type:Trading Company

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Shandong Mopai Biotechnology Co., LTD

Shandong Mopai Biotechnology Co., LTD is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemicals. W

Homovanillyl alcohol CAS NO.2380-78-1

Cas:2380-78-1

Min.Order:1 Gram

Negotiable

Type:Lab/Research institutions

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KAISA GROUP INC

1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer

Homovanillyl alcohol CAS NO.2380-78-1

Cas:2380-78-1

Min.Order:1 Metric Ton

FOB Price: $1.5

Type:Trading Company

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Hunan chemfish Pharmaceutical co.,Ltd

Appearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea

4-Hydroxy-3-methoxyphenethanol

Cas:2380-78-1

Min.Order:0

Negotiable

Type:Manufacturers

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Bluecrystal chem-union

We are a Union of chemistry in China, consists of chemists,engineers, laboratories,factories in China. We organize surplus capacity of R&D and production as well as custom synthesis for chemical products and chemical business project. We are supp

Homovanillyl alcohol CAS NO.2380-78-1

Cas:2380-78-1

Min.Order:1 Metric Ton

FOB Price: $1.0

Type:Trading Company

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Hebei Mojin Biotechnology Co.,Ltd

1, High quality with competitive price:2, Fast and safe delivery3.Excellent pre-sales and after-sales service4. Well-trained and professional technologist and sales with rich experience in the field for 5-10 yearsAppearance:see detailed specification

Benzeneethanol,4-hydroxy-3-methoxy-

Cas:2380-78-1

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Hangzhou Dingyan Chem Co., Ltd

R & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates

Benzeneethanol,4-hydroxy-3-methoxy-

Cas:2380-78-1

Min.Order:0

Negotiable

Type:Manufacturers

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DB BIOTECH CO., LTD

Q1: Are you a manufacturer Answer: Yes, we are factory founded on 2012.Q2: How to contact with us Click "contact supplier" And then send us message the product you interest in, you will get reply within 12 hours.Q3:Which kind of payment terms do you

Homovanillyl alcohol

Cas:2380-78-1

Min.Order:0

Negotiable

Type:Trading Company

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Xian Changyue Biological Technology Co., Ltd.

best seller Application:API

Homovanillyl alcohol

Cas:2380-78-1

Min.Order:0

Negotiable

Type:Manufacturers

inquiry

Hebei Sankai Chemical Technology Co., Ltd

1. Product advantages? High purity, all above 98.5%, no impurities after dissolution? We will test each batch to ensure quality? OEM and private brand services designed for free? Various cap colors available? We can also provide MT1 peptide powder2.

Homovanillyl alcohol

Cas:2380-78-1

Min.Order:0

Negotiable

Type:Trading Company

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Antimex Chemical Limied

Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali

Benzeneethanol,4-hydroxy-3-methoxy-

Cas:2380-78-1

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Hubei Langyou International Trading Co., Ltd

Homovanillyl alcohol CAS NO.2380-78-1 Application:Homovanillyl alcohol CAS NO.2380-78-1

Homovanillyl alcohol CAS NO.2380-78-1

Cas:2380-78-1

Min.Order:0

Negotiable

Type:Other

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Hangzhou Fandachem Co.,Ltd

4-HYDROXY-3-METHOXYPHENETHANOLAppearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express

4-HYDROXY-3-METHOXYPHENETHANOL

Cas:2380-78-1

Min.Order:0

Negotiable

Type:Other

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Hangzhou Sartort Biopharma Co., Ltd

Best quality with low priceAppearance:yellow to light brown crystalline chunks Storage:ln stock Package:25kg/Barrel Application:Chemicals Transportation:Express/Sea/Air Port:Shanghai

Homovanillyl alcohol

Cas:2380-78-1

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Henan Kanbei Chemical Co.,LTD

factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin

Homovanillyl alcohol

Cas:2380-78-1

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Shanghai Chinqesen Biotechnology Co., Ltd.

Good Quality Package:1kg/bag Application:Medical or chemical Transportation:Air/Train/Sea Port:Shenzhen

2380-78-1

Cas:2380-78-1

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Hebei Quanhe Biotechnology Co. LTD

1. Timely and efficient service to ensure communication with customers2. Produce products of different specifications and sizes according to your requirements.3. Quality procedures and standards recognized by SGS. Advanced plant equipment ensures sta

Homovanillyl alcohol

Cas:2380-78-1

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Hunan Longxianng Runhui Trading Co.,Ltd

Homovanillyl alcohol CAS NO.2380-78-1Appearance:please contact me Storage:Keep in dry and cool place Package:foil bags, drums or bottles Application:Steroids, Cosmetics Ingredients, APIs Transportation:By express (Door to door) such as FEDEX, DHL, EM

Homovanillyl alcohol CAS NO.2380-78-1

Cas:2380-78-1

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Shanghai Yuanye Bio-Technology Co., Ltd.

good quality, competitive price, thoughtful after sale serviceAppearance:white powder Storage:Keep it in dry,shady and cool place Package:5mg Application:Pharma;Industry;Agricultural;chemical reaserch Transportation:by express or by sea Port:Any port

Vanillylmethanol

Cas:2380-78-1

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Synthetic route

tert-butyl 4-(2-tert-butoxyethyl)-2-methoxyphenyl carbonate

tert-butyl 4-(2-tert-butoxyethyl)-2-methoxyphenyl carbonate

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
With erbium(III) triflate In ethanol for 50h; Microwave irradiation;98%
4-allylguaiacol
97-53-0

4-allylguaiacol

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
Stage #1: 4-allylguaiacol With ozone In ethanol at -55℃;
Stage #2: With sodium tetrahydroborate In ethyl acetate at 20℃;
98%
Multi-step reaction with 2 steps
1: ozone / sodium hydrogencarbonate / dichloromethane; methanol / 2 h / -78 °C
2: sodium tetrahydroborate; methanol / dichloromethane / 2 h / -78 - 20 °C / Inert atmosphere
View Scheme
sodium methylate
124-41-4

sodium methylate

3-bromo-4-hydroxyphenylethyl alcohol
196081-78-4

3-bromo-4-hydroxyphenylethyl alcohol

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
With copper(I) bromide In N,N-dimethyl-formamide at 120℃; for 1h;97.3%
Stage #1: sodium methylate With copper(I) bromide In methanol; N,N-dimethyl-formamide
Stage #2: 3-bromo-4-hydroxyphenylethyl alcohol In methanol; N,N-dimethyl-formamide at 100℃; Temperature;
92%
With methanol; copper(I) bromide In N,N-dimethyl-formamide at 90℃; for 3h;87.6%
With copper(I) bromide In water; N,N-dimethyl-formamide
copper(I) bromide In methanol; N,N-dimethyl-formamide at 120℃;
tert-butyl 4-(2-hydroxyethyl)-2-methoxyphenyl carbonate

tert-butyl 4-(2-hydroxyethyl)-2-methoxyphenyl carbonate

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
With erbium(III) triflate In ethanol for 50h; Microwave irradiation;94%
C21H40O3Si2
1044264-42-7

C21H40O3Si2

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
With methanol; trimethylsilyl bromide at 20℃; for 5h; chemoselective reaction;92%
(E)-3-(4-hydroxy-3-methoxyphenyl)acrylic acid
1135-24-6

(E)-3-(4-hydroxy-3-methoxyphenyl)acrylic acid

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
With β-D-glucose; oxygen In aq. phosphate buffer at 37℃; for 18h; pH=7.0; Enzymatic reaction;91.9%
Multi-step reaction with 4 steps
1: Bacillus licheniformis strain CGMCC 7172 phenolic acid decarboxylase / 6 h / Enzymatic reaction
2: oxygen; β-D-glucose; styrene monooxygenase (AF031161.1) from Pseudomonas sp. VLB120 / Enzymatic reaction
3: styrene oxide isomerase (KF540254.1) from Rhodococcus opacus 1CP / Enzymatic reaction
4: alcohol dehydrogenase (NC_001145.3) from Saccharomyces cerevisiae S288C
View Scheme
1-<4-(benzyloxy)-3-methoxyphenyl>ethan-2-ol
64881-05-6

1-<4-(benzyloxy)-3-methoxyphenyl>ethan-2-ol

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
With hydrogen; palladium on activated charcoal In methanol under 750.06 Torr; for 1h;91%
ethyl homovanillate
60563-13-5

ethyl homovanillate

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
With lithium aluminium tetrahydride In tetrahydrofuran at 0℃; for 3h; Inert atmosphere; Reflux;89%
methanol
67-56-1

methanol

cistanoside C
94492-22-5

cistanoside C

A

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

B

Methyl caffeate
3843-74-1, 67667-67-8

Methyl caffeate

Conditions
ConditionsYield
With acetyl chloride for 0.5h; Heating;
methanol
67-56-1

methanol

cistanoside D
94492-21-4

cistanoside D

A

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

B

Methyl ferulate
2309-07-1

Methyl ferulate

Conditions
ConditionsYield
With acetyl chloride for 0.5h; Heating;
cistanoside
93236-41-0

cistanoside

acetyl chloride
75-36-5

acetyl chloride

A

methyl (E)-3-(3-hydroxy-4-methoxyphenyl)-2-propenoate
97966-29-5

methyl (E)-3-(3-hydroxy-4-methoxyphenyl)-2-propenoate

B

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
In methanol for 0.5h; Heating; Title compound not separated from byproducts;
cistanoside

cistanoside

acetyl chloride
75-36-5

acetyl chloride

A

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

B

Methyl caffeate
3843-74-1, 67667-67-8

Methyl caffeate

Conditions
ConditionsYield
In methanol for 0.5h; Heating; Title compound not separated from byproducts;
oxirane
75-21-8

oxirane

4-bromoguaiacol
7368-78-7

4-bromoguaiacol

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
(i) nBuLi, Et2O, (ii) /BRN= 102378/, Et2O, benzene; Multistep reaction;
2-benzyloxy-5-bromoanisole
63057-72-7

2-benzyloxy-5-bromoanisole

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 1.) Mg, 1,2-dibromoethane, 2.) 1,5-cyclooctadiene copper(I) chloride / 1.) THF, reflux, 5 h, 2.) THF, 0 deg C - 14 deg C, 16 h
2: 91 percent / H2 / 5percent Pd/C / methanol / 1 h / 750.06 Torr
View Scheme
tert-butyl 4-(2-tert-butoxyethyl)-2-methoxyphenyl carbonate

tert-butyl 4-(2-tert-butoxyethyl)-2-methoxyphenyl carbonate

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
With erbium(III) triflate In ethanol for 50h; Microwave irradiation;98%
4-allylguaiacol
97-53-0

4-allylguaiacol

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
Stage #1: 4-allylguaiacol With ozone In ethanol at -55℃;
Stage #2: With sodium tetrahydroborate In ethyl acetate at 20℃;
98%
Multi-step reaction with 2 steps
1: ozone / sodium hydrogencarbonate / dichloromethane; methanol / 2 h / -78 °C
2: sodium tetrahydroborate; methanol / dichloromethane / 2 h / -78 - 20 °C / Inert atmosphere
View Scheme
sodium methylate
124-41-4

sodium methylate

3-bromo-4-hydroxyphenylethyl alcohol
196081-78-4

3-bromo-4-hydroxyphenylethyl alcohol

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
With copper(I) bromide In N,N-dimethyl-formamide at 120℃; for 1h;97.3%
Stage #1: sodium methylate With copper(I) bromide In methanol; N,N-dimethyl-formamide
Stage #2: 3-bromo-4-hydroxyphenylethyl alcohol In methanol; N,N-dimethyl-formamide at 100℃; Temperature;
92%
With methanol; copper(I) bromide In N,N-dimethyl-formamide at 90℃; for 3h;87.6%
With copper(I) bromide In water; N,N-dimethyl-formamide
copper(I) bromide In methanol; N,N-dimethyl-formamide at 120℃;
tert-butyl 4-(2-hydroxyethyl)-2-methoxyphenyl carbonate

tert-butyl 4-(2-hydroxyethyl)-2-methoxyphenyl carbonate

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
With erbium(III) triflate In ethanol for 50h; Microwave irradiation;94%
C21H40O3Si2
1044264-42-7

C21H40O3Si2

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
With methanol; trimethylsilyl bromide at 20℃; for 5h; chemoselective reaction;92%
(E)-3-(4-hydroxy-3-methoxyphenyl)acrylic acid
1135-24-6

(E)-3-(4-hydroxy-3-methoxyphenyl)acrylic acid

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
With β-D-glucose; oxygen In aq. phosphate buffer at 37℃; for 18h; pH=7.0; Enzymatic reaction;91.9%
Multi-step reaction with 4 steps
1: Bacillus licheniformis strain CGMCC 7172 phenolic acid decarboxylase / 6 h / Enzymatic reaction
2: oxygen; β-D-glucose; styrene monooxygenase (AF031161.1) from Pseudomonas sp. VLB120 / Enzymatic reaction
3: styrene oxide isomerase (KF540254.1) from Rhodococcus opacus 1CP / Enzymatic reaction
4: alcohol dehydrogenase (NC_001145.3) from Saccharomyces cerevisiae S288C
View Scheme
1-<4-(benzyloxy)-3-methoxyphenyl>ethan-2-ol
64881-05-6

1-<4-(benzyloxy)-3-methoxyphenyl>ethan-2-ol

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
With hydrogen; palladium on activated charcoal In methanol under 750.06 Torr; for 1h;91%
ethyl homovanillate
60563-13-5

ethyl homovanillate

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
With lithium aluminium tetrahydride In tetrahydrofuran at 0℃; for 3h; Inert atmosphere; Reflux;89%
methanol
67-56-1

methanol

cistanoside C
94492-22-5

cistanoside C

A

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

B

Methyl caffeate
3843-74-1, 67667-67-8

Methyl caffeate

Conditions
ConditionsYield
With acetyl chloride for 0.5h; Heating;
methanol
67-56-1

methanol

cistanoside D
94492-21-4

cistanoside D

A

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

B

Methyl ferulate
2309-07-1

Methyl ferulate

Conditions
ConditionsYield
With acetyl chloride for 0.5h; Heating;
cistanoside
93236-41-0

cistanoside

acetyl chloride
75-36-5

acetyl chloride

A

methyl (E)-3-(3-hydroxy-4-methoxyphenyl)-2-propenoate
97966-29-5

methyl (E)-3-(3-hydroxy-4-methoxyphenyl)-2-propenoate

B

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
In methanol for 0.5h; Heating; Title compound not separated from byproducts;
cistanoside

cistanoside

acetyl chloride
75-36-5

acetyl chloride

A

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

B

Methyl caffeate
3843-74-1, 67667-67-8

Methyl caffeate

Conditions
ConditionsYield
In methanol for 0.5h; Heating; Title compound not separated from byproducts;
oxirane
75-21-8

oxirane

4-bromoguaiacol
7368-78-7

4-bromoguaiacol

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
(i) nBuLi, Et2O, (ii) /BRN= 102378/, Et2O, benzene; Multistep reaction;
2-benzyloxy-5-bromoanisole
63057-72-7

2-benzyloxy-5-bromoanisole

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 1.) Mg, 1,2-dibromoethane, 2.) 1,5-cyclooctadiene copper(I) chloride / 1.) THF, reflux, 5 h, 2.) THF, 0 deg C - 14 deg C, 16 h
2: 91 percent / H2 / 5percent Pd/C / methanol / 1 h / 750.06 Torr
View Scheme
1-tert-butoxy-4-(2-tert-butoxyethyl)-2-methoxybenzene
1286729-19-8

1-tert-butoxy-4-(2-tert-butoxyethyl)-2-methoxybenzene

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
With erbium(III) triflate In methanol at 100℃; for 0.75h; Microwave irradiation;
2-(4-hydroxy-3-methoxyphenyl)acetaldehyde
5703-24-2

2-(4-hydroxy-3-methoxyphenyl)acetaldehyde

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
With methanol; sodium tetrahydroborate In dichloromethane at -78 - 20℃; for 2h; Inert atmosphere;
With alcohol dehydrogenase (NC_001145.3) from Saccharomyces cerevisiae S288C
lignin acetosolv type

lignin acetosolv type

A

4-n-Propylphenol
645-56-7

4-n-Propylphenol

B

2-Methoxy-4-methylphenol
93-51-6

2-Methoxy-4-methylphenol

C

2-methoxy-4-n-propylphenol
2785-87-7

2-methoxy-4-n-propylphenol

D

2-methoxy-4-propenylphenol
97-54-1

2-methoxy-4-propenylphenol

E

4-Ethylguaiacol
2785-89-9

4-Ethylguaiacol

F

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

G

4-propylbenzene-1,2-diol
2525-02-2

4-propylbenzene-1,2-diol

H

benzene-1,2-diol
120-80-9

benzene-1,2-diol

I

2-methoxy-phenol
90-05-1

2-methoxy-phenol

J

4-methyl-1,2-dihydroxybenzene
452-86-8

4-methyl-1,2-dihydroxybenzene

Conditions
ConditionsYield
With 5% palladium on Al2O3; hydrogen In water at 25 - 310℃; under 37503.8 Torr; for 1h; Autoclave;
p-hydroxyphenethyl alcohol
501-94-0

p-hydroxyphenethyl alcohol

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: sodium bromide; oxone / acetone; water / 20 °C
2.1: copper(I) bromide / N,N-dimethyl-formamide; methanol
2.2: 100 °C
View Scheme
Multi-step reaction with 2 steps
1: sodium bromide; oxone||potassium monopersulfate triple salt / acetone; water / 15 h / 0 °C
2: copper(I) bromide; methanol / N,N-dimethyl-formamide / 3 h / 90 °C
View Scheme
Multi-step reaction with 2 steps
1.1: N-Bromosuccinimide / methanol / 3 h / 20 °C
2.1: copper(I) bromide; sodium methylate / methanol / 15 h / 100 °C
2.2: 12 h / 20 °C
View Scheme
2-(3,4-dihydroxyphenyl)acetic acid methyl ester
25379-88-8

2-(3,4-dihydroxyphenyl)acetic acid methyl ester

A

2-(3-hydroxy-4-methoxyphenyl)ethanol
50602-41-0

2-(3-hydroxy-4-methoxyphenyl)ethanol

B

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: toluene-4-sulfonic acid / dichloromethane / 8 h / Inert atmosphere; Darkness; Reflux
2: lithium aluminium tetrahydride / diethyl ether / 3 h / 0 °C / Inert atmosphere
3: Amberlyst 15 / methanol / 8 h / Reflux
4: methyltransferase I from Desulfitobacterium hafniense / methanol / 24 h / 30 °C / pH 6.5 / Inert atmosphere; Glovebox; Enzymatic reaction
View Scheme
hydroxytyrosol
10597-60-1

hydroxytyrosol

2-methoxy-phenol
90-05-1

2-methoxy-phenol

A

2-(3-hydroxy-4-methoxyphenyl)ethanol
50602-41-0

2-(3-hydroxy-4-methoxyphenyl)ethanol

B

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
With methyltransferase I from Desulfitobacterium hafniense In methanol at 30℃; for 24h; pH=6.5; Solvent; Inert atmosphere; Glovebox; Enzymatic reaction; regioselective reaction;
2-(2,2-dimethylbenzo[1,3]dioxol-5-yl)acetic acid methyl ester
38515-62-7

2-(2,2-dimethylbenzo[1,3]dioxol-5-yl)acetic acid methyl ester

A

2-(3-hydroxy-4-methoxyphenyl)ethanol
50602-41-0

2-(3-hydroxy-4-methoxyphenyl)ethanol

B

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: lithium aluminium tetrahydride / diethyl ether / 3 h / 0 °C / Inert atmosphere
2: Amberlyst 15 / methanol / 8 h / Reflux
3: methyltransferase I from Desulfitobacterium hafniense / methanol / 24 h / 30 °C / pH 6.5 / Inert atmosphere; Glovebox; Enzymatic reaction
View Scheme
2-(2,2-dimethylbenzo[d][1,3]dioxol-5-yl)ethan-1-ol
119054-91-0

2-(2,2-dimethylbenzo[d][1,3]dioxol-5-yl)ethan-1-ol

A

2-(3-hydroxy-4-methoxyphenyl)ethanol
50602-41-0

2-(3-hydroxy-4-methoxyphenyl)ethanol

B

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: Amberlyst 15 / methanol / 8 h / Reflux
2: methyltransferase I from Desulfitobacterium hafniense / methanol / 24 h / 30 °C / pH 6.5 / Inert atmosphere; Glovebox; Enzymatic reaction
View Scheme
3,4-dihydroxyphenylacetate
102-32-9

3,4-dihydroxyphenylacetate

A

2-(3-hydroxy-4-methoxyphenyl)ethanol
50602-41-0

2-(3-hydroxy-4-methoxyphenyl)ethanol

B

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
Multi-step reaction with 5 steps
1: sulfuric acid / 2 h / Inert atmosphere; Darkness; Reflux
2: toluene-4-sulfonic acid / dichloromethane / 8 h / Inert atmosphere; Darkness; Reflux
3: lithium aluminium tetrahydride / diethyl ether / 3 h / 0 °C / Inert atmosphere
4: Amberlyst 15 / methanol / 8 h / Reflux
5: methyltransferase I from Desulfitobacterium hafniense / methanol / 24 h / 30 °C / pH 6.5 / Inert atmosphere; Glovebox; Enzymatic reaction
View Scheme
dewaxed lignin from Chinese quince fruits (Chaenomeles sinensis), extracted at 200 °C over 90 min by 60percent ethanol-water mixture

dewaxed lignin from Chinese quince fruits (Chaenomeles sinensis), extracted at 200 °C over 90 min by 60percent ethanol-water mixture

A

3,4-dimethoxyphenol
2033-89-8

3,4-dimethoxyphenol

B

4-allylguaiacol
97-53-0

4-allylguaiacol

C

1,3-dimethoxy-2-hydroxy-benzene
91-10-1

1,3-dimethoxy-2-hydroxy-benzene

D

2-Methoxy-4-methylphenol
93-51-6

2-Methoxy-4-methylphenol

E

2-methoxy-4-n-propylphenol
2785-87-7

2-methoxy-4-n-propylphenol

F

3-methocycatechol
934-00-9

3-methocycatechol

G

1,2,3-trimethoxybenzene
634-36-6

1,2,3-trimethoxybenzene

H

2,4,6-trihydroxyacetophenone
480-66-0

2,4,6-trihydroxyacetophenone

I

4-allyl-2,6-dimethoxyphenol
6627-88-9

4-allyl-2,6-dimethoxyphenol

J

1-(4-hydroxy-3,5-dimethoxy-phenyl)-ethanone
2478-38-8

1-(4-hydroxy-3,5-dimethoxy-phenyl)-ethanone

K

3-methoxy-4-hydroxystyrene
7786-61-0

3-methoxy-4-hydroxystyrene

L

4-Ethylguaiacol
2785-89-9

4-Ethylguaiacol

M

1-(4-hydroxy-3-methoxyphenyl)2-propanone
2503-46-0

1-(4-hydroxy-3-methoxyphenyl)2-propanone

N

1-(2,4,6-trihydroxy-3-methylphenyl)butan-1-one
1509-06-4

1-(2,4,6-trihydroxy-3-methylphenyl)butan-1-one

O

3-hydroxy-5-tert-butyl-catechol
20481-17-8

3-hydroxy-5-tert-butyl-catechol

P

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Q

benzene-1,2-diol
120-80-9

benzene-1,2-diol

R

2-methoxy-phenol
90-05-1

2-methoxy-phenol

S

4-methyl-1,2-dihydroxybenzene
452-86-8

4-methyl-1,2-dihydroxybenzene

T

syringic aldehyde
134-96-3

syringic aldehyde

U

phenol
108-95-2

phenol

Conditions
ConditionsYield
at 500℃; for 0.00555556h; Pyrolysis;
dewaxed lignin from Chinese quince fruits (Chaenomeles sinensis), extracted at 240 °C over 90 min by 60percent ethanol-water mixture

dewaxed lignin from Chinese quince fruits (Chaenomeles sinensis), extracted at 240 °C over 90 min by 60percent ethanol-water mixture

A

4-allylguaiacol
97-53-0

4-allylguaiacol

B

1,3-dimethoxy-2-hydroxy-benzene
91-10-1

1,3-dimethoxy-2-hydroxy-benzene

C

2-Methoxy-4-methylphenol
93-51-6

2-Methoxy-4-methylphenol

D

2-methoxy-4-n-propylphenol
2785-87-7

2-methoxy-4-n-propylphenol

E

2,3-Dimethylphenol
526-75-0

2,3-Dimethylphenol

F

3-methocycatechol
934-00-9

3-methocycatechol

G

1,2,3-trimethoxybenzene
634-36-6

1,2,3-trimethoxybenzene

H

2,6-dihydroxy-4-methoxy-acetophenone
7507-89-3

2,6-dihydroxy-4-methoxy-acetophenone

I

4-allyl-2,6-dimethoxyphenol
6627-88-9

4-allyl-2,6-dimethoxyphenol

J

1-(4-hydroxy-3,5-dimethoxy-phenyl)-ethanone
2478-38-8

1-(4-hydroxy-3,5-dimethoxy-phenyl)-ethanone

K

3-methoxy-4-hydroxystyrene
7786-61-0

3-methoxy-4-hydroxystyrene

L

4-Ethylguaiacol
2785-89-9

4-Ethylguaiacol

M

1-(4-hydroxy-3-methoxyphenyl)2-propanone
2503-46-0

1-(4-hydroxy-3-methoxyphenyl)2-propanone

N

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

O

benzene-1,2-diol
120-80-9

benzene-1,2-diol

P

2-methoxy-phenol
90-05-1

2-methoxy-phenol

Q

syringic aldehyde
134-96-3

syringic aldehyde

R

phenol
108-95-2

phenol

Conditions
ConditionsYield
at 500℃; for 0.00555556h; Pyrolysis;
p-hydroxyphenethyl alcohol
501-94-0

p-hydroxyphenethyl alcohol

A

2-(4'-hydroxy-3'-methoxyphenyl)ethyl methyl carbonate
953422-35-0

2-(4'-hydroxy-3'-methoxyphenyl)ethyl methyl carbonate

B

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: N-Bromosuccinimide / methanol / 3 h / 20 °C
2: copper(I) bromide; sodium methylate / methanol / 15 h / 100 °C
View Scheme
carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

3-bromo-4-hydroxyphenylethyl alcohol
196081-78-4

3-bromo-4-hydroxyphenylethyl alcohol

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
Stage #1: carbonic acid dimethyl ester; 3-bromo-4-hydroxyphenylethyl alcohol With sodium methylate; copper(I) bromide In methanol at 100℃; for 15h;
Stage #2: With potassium carbonate In methanol at 20℃; for 12h;
carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

3-bromo-4-hydroxyphenylethyl alcohol
196081-78-4

3-bromo-4-hydroxyphenylethyl alcohol

A

2-(4'-hydroxy-3'-methoxyphenyl)ethyl methyl carbonate
953422-35-0

2-(4'-hydroxy-3'-methoxyphenyl)ethyl methyl carbonate

B

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

Conditions
ConditionsYield
With sodium methylate; copper(I) bromide In methanol at 100℃; for 15h;
1-(3,4-dimethoxyphenyl)-5-hydroxydecan-3-one
61914-52-1

1-(3,4-dimethoxyphenyl)-5-hydroxydecan-3-one

A

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

B

C18H28O5

C18H28O5

C

C18H30O5

C18H30O5

D

C18H30O5

C18H30O5

E

2-(3,4-dimethoxyphenyl)ethyl alcohol
7417-21-2

2-(3,4-dimethoxyphenyl)ethyl alcohol

Conditions
ConditionsYield
With Colletotrichum gloeosporioides In water; dimethyl sulfoxide at 30℃; for 120h; Microbiological reaction;
homovanillyl alcohol
2380-78-1

homovanillyl alcohol

acetic anhydride
108-24-7

acetic anhydride

4-(2-acetoxyethyl)-2-methoxy-1-acetoxy-benzene
32022-28-9

4-(2-acetoxyethyl)-2-methoxy-1-acetoxy-benzene

Conditions
ConditionsYield
In neat (no solvent) Molecular sieve; Microwave irradiation; Green chemistry;100%
With acetic acid at 50℃;95%
With acetic acid at 50℃;95.3%
With pyridine95%
With acetic acid at 50℃; for 12h;67%
homovanillyl alcohol
2380-78-1

homovanillyl alcohol

carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

2-(4'-hydroxy-3'-methoxyphenyl)ethyl methyl carbonate
953422-35-0

2-(4'-hydroxy-3'-methoxyphenyl)ethyl methyl carbonate

Conditions
ConditionsYield
With sulfuric acid for 7h; Reflux;100%
With 1,8-diazabicyclo[5.4.0]undec-7-ene at 90℃; for 7.5h;98%
homovanillyl alcohol
2380-78-1

homovanillyl alcohol

tert-butyldimethylsilyl chloride
18162-48-6

tert-butyldimethylsilyl chloride

C21H40O3Si2
1044264-42-7

C21H40O3Si2

Conditions
ConditionsYield
With triethylamine In N,N-dimethyl-formamide at 20℃; for 3h;100%
With 1H-imidazole
homovanillyl alcohol
2380-78-1

homovanillyl alcohol

acetyl chloride
75-36-5

acetyl chloride

2-(4'-hydroxy-3'-methoxyphenyl)ethyl acetate

2-(4'-hydroxy-3'-methoxyphenyl)ethyl acetate

Conditions
ConditionsYield
In carbonic acid dimethyl ester at 20℃; for 24h;100%
vinyl propionate
105-38-4

vinyl propionate

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

C12H16O4

C12H16O4

Conditions
ConditionsYield
With Candida antarctica lipase In various solvent(s) at 40℃; for 1.5h;98.1%
vinyl stearate
111-63-7

vinyl stearate

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

4-hydroxy-3-methoxyphenethyl stearate

4-hydroxy-3-methoxyphenethyl stearate

Conditions
ConditionsYield
With Candida antarctica lipase In various solvent(s) at 40℃; for 4h;98%
homovanillyl alcohol
2380-78-1

homovanillyl alcohol

benzaldehyde
100-52-7

benzaldehyde

6-methoxy-1-phenylisochroman-7-ol

6-methoxy-1-phenylisochroman-7-ol

Conditions
ConditionsYield
With sulfuric acid at 20℃;98%
vinyl caprate
4704-31-8

vinyl caprate

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

C19H30O4

C19H30O4

Conditions
ConditionsYield
With Candida antarctica lipase In various solvent(s) at 40℃; for 1.5h;97.5%
homovanillyl alcohol
2380-78-1

homovanillyl alcohol

hydroxytyrosol
10597-60-1

hydroxytyrosol

Conditions
ConditionsYield
With 3-mercaptopropionic acid ethyl ester In aq. buffer at 30℃; for 24h; pH=6.5; Inert atmosphere; Glovebox; Enzymatic reaction;97%
Stage #1: homovanillyl alcohol With aluminum (III) chloride In ethanethiol at 0 - 20℃; for 42h;
Stage #2: With hydrogenchloride; water Cooling with ice;
94.7%
With sodium periodate In water; ethyl acetate Concentration; Reagent/catalyst; Temperature; Solvent; Time;78%
vinyl acetate
108-05-4

vinyl acetate

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

2-(4'-hydroxy-3'-methoxyphenyl)ethyl acetate

2-(4'-hydroxy-3'-methoxyphenyl)ethyl acetate

Conditions
ConditionsYield
With Candida antarctica lipase In various solvent(s) at 40℃; for 1h;96.8%
With Candida antarctica lipase In tert-butyl methyl ether at 40℃; Enzymatic reaction;96.5%
1-Bromo-3-phenylpropane
637-59-2

1-Bromo-3-phenylpropane

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

2-[3-methoxy-4-(3-phenylpropoxy)phenyl]ethanol

2-[3-methoxy-4-(3-phenylpropoxy)phenyl]ethanol

Conditions
ConditionsYield
With potassium carbonate In acetonitrile for 7h; Reflux;95%
8-methylnonanoic acid
5963-14-4

8-methylnonanoic acid

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

8-methylnonanoic acid 2-(4-hydroxy-3-methoxyphenyl)ethyl ester
951221-74-2

8-methylnonanoic acid 2-(4-hydroxy-3-methoxyphenyl)ethyl ester

Conditions
ConditionsYield
novozyme 435 at 50℃; for 16h; Enzymatic reaction; Neat (no solvent);93.2%
homovanillyl alcohol
2380-78-1

homovanillyl alcohol

allyl bromide
106-95-6

allyl bromide

C12H16O3

C12H16O3

Conditions
ConditionsYield
With potassium carbonate In acetone Reflux;93%
homovanillyl alcohol
2380-78-1

homovanillyl alcohol

methyl iodide
74-88-4

methyl iodide

2-(3,4-dimethoxyphenyl)ethyl alcohol
7417-21-2

2-(3,4-dimethoxyphenyl)ethyl alcohol

Conditions
ConditionsYield
With sodium hydride In N,N-dimethyl-formamide for 0.5h;93%
di-tert-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

tert-butyl 4-(2-tert-butoxyethyl)-2-methoxyphenyl carbonate

tert-butyl 4-(2-tert-butoxyethyl)-2-methoxyphenyl carbonate

Conditions
ConditionsYield
With mesoporous silica MCM-41 supported erbium(III) at 40℃; for 9h; Neat (no solvent); ultrasound irradiation; Inert atmosphere;92%
vinyl n-butyrate
123-20-6

vinyl n-butyrate

homovanillyl alcohol
2380-78-1

homovanillyl alcohol

C13H18O4

C13H18O4

Conditions
ConditionsYield
With Candida antarctica lipase In various solvent(s) at 40℃; for 1.5h;90.9%
homovanillyl alcohol
2380-78-1

homovanillyl alcohol

UDP-glucuronic acid
2616-64-0

UDP-glucuronic acid

A

2-[3′-hydroxy-4′-(β-D-glucopyranosyluronic acid)phenyl]ethanol

2-[3′-hydroxy-4′-(β-D-glucopyranosyluronic acid)phenyl]ethanol

B

homovanillic alcohol 1-O-β-D-glucuronide

homovanillic alcohol 1-O-β-D-glucuronide

Conditions
ConditionsYield
With Tris-HCl buffer; calcium chloride; diothiothreitol; benzenesulfonamide; uridine 5'-diphosphoglucuronyl transferases (porcine liver) In water; dimethyl sulfoxide at 35℃; for 6h; pH=8.0; Enzymatic reaction;A 88%
B 6.1%
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