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
Cas:2380-78-1
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
inquiryXi'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,
Cas:2380-78-1
Min.Order:1 Kilogram
FOB Price: $52.0 / 55.0
Type:Other
inquiryOur 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
Cas:2380-78-1
Min.Order:1 Kilogram
FOB Price: $1.0 / 10.0
Type:Trading Company
inquiryWITH 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
Cas:2380-78-1
Min.Order:1 Kilogram
FOB Price: $139.0 / 210.0
Type:Trading Company
inquiry1.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
Cas:2380-78-1
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiryHomovanillyl 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
Cas:2380-78-1
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiryHello, 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
Cas:2380-78-1
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryHenan 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
Cas:2380-78-1
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryJ&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
Cas:2380-78-1
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryZibo 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
Cas:2380-78-1
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
inquiryOur 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
Cas:2380-78-1
Min.Order:1 Metric Ton
FOB Price: $5000.0
Type:Lab/Research institutions
inquiryfactory?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
Cas:2380-78-1
Min.Order:1 Kilogram
FOB Price: $18.0 / 20.0
Type:Trading Company
inquiryShandong 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
Cas:2380-78-1
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiry1.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
Cas:2380-78-1
Min.Order:1 Metric Ton
FOB Price: $1.5
Type:Trading Company
inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
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
Cas:2380-78-1
Min.Order:1 Metric Ton
FOB Price: $1.0
Type:Trading Company
inquiry1, 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
Cas:2380-78-1
Min.Order:0
Negotiable
Type:Trading Company
inquiryR & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates
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
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.
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
Cas:2380-78-1
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryHomovanillyl alcohol CAS NO.2380-78-1 Application:Homovanillyl alcohol CAS NO.2380-78-1
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
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
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Good Quality Package:1kg/bag Application:Medical or chemical Transportation:Air/Train/Sea Port:Shenzhen
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 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
Cas:2380-78-1
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquirygood 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
homovanillyl alcohol
Conditions | Yield |
---|---|
With erbium(III) triflate In ethanol for 50h; Microwave irradiation; | 98% |
Conditions | Yield |
---|---|
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
3-bromo-4-hydroxyphenylethyl alcohol
homovanillyl alcohol
Conditions | Yield |
---|---|
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℃; |
homovanillyl alcohol
Conditions | Yield |
---|---|
With erbium(III) triflate In ethanol for 50h; Microwave irradiation; | 94% |
C21H40O3Si2
homovanillyl alcohol
Conditions | Yield |
---|---|
With methanol; trimethylsilyl bromide at 20℃; for 5h; chemoselective reaction; | 92% |
Conditions | Yield |
---|---|
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
homovanillyl alcohol
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In methanol under 750.06 Torr; for 1h; | 91% |
ethyl homovanillate
homovanillyl alcohol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran at 0℃; for 3h; Inert atmosphere; Reflux; | 89% |
methanol
cistanoside C
A
homovanillyl alcohol
B
Methyl caffeate
Conditions | Yield |
---|---|
With acetyl chloride for 0.5h; Heating; |
methanol
cistanoside D
A
homovanillyl alcohol
B
Methyl ferulate
Conditions | Yield |
---|---|
With acetyl chloride for 0.5h; Heating; |
cistanoside
acetyl chloride
A
methyl (E)-3-(3-hydroxy-4-methoxyphenyl)-2-propenoate
B
homovanillyl alcohol
Conditions | Yield |
---|---|
In methanol for 0.5h; Heating; Title compound not separated from byproducts; |
Conditions | Yield |
---|---|
In methanol for 0.5h; Heating; Title compound not separated from byproducts; |
Conditions | Yield |
---|---|
(i) nBuLi, Et2O, (ii) /BRN= 102378/, Et2O, benzene; Multistep reaction; |
2-benzyloxy-5-bromoanisole
homovanillyl alcohol
Conditions | Yield |
---|---|
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 |
homovanillyl alcohol
Conditions | Yield |
---|---|
With erbium(III) triflate In ethanol for 50h; Microwave irradiation; | 98% |
Conditions | Yield |
---|---|
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
3-bromo-4-hydroxyphenylethyl alcohol
homovanillyl alcohol
Conditions | Yield |
---|---|
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℃; |
homovanillyl alcohol
Conditions | Yield |
---|---|
With erbium(III) triflate In ethanol for 50h; Microwave irradiation; | 94% |
C21H40O3Si2
homovanillyl alcohol
Conditions | Yield |
---|---|
With methanol; trimethylsilyl bromide at 20℃; for 5h; chemoselective reaction; | 92% |
Conditions | Yield |
---|---|
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
homovanillyl alcohol
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In methanol under 750.06 Torr; for 1h; | 91% |
ethyl homovanillate
homovanillyl alcohol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran at 0℃; for 3h; Inert atmosphere; Reflux; | 89% |
methanol
cistanoside C
A
homovanillyl alcohol
B
Methyl caffeate
Conditions | Yield |
---|---|
With acetyl chloride for 0.5h; Heating; |
methanol
cistanoside D
A
homovanillyl alcohol
B
Methyl ferulate
Conditions | Yield |
---|---|
With acetyl chloride for 0.5h; Heating; |
cistanoside
acetyl chloride
A
methyl (E)-3-(3-hydroxy-4-methoxyphenyl)-2-propenoate
B
homovanillyl alcohol
Conditions | Yield |
---|---|
In methanol for 0.5h; Heating; Title compound not separated from byproducts; |
Conditions | Yield |
---|---|
In methanol for 0.5h; Heating; Title compound not separated from byproducts; |
Conditions | Yield |
---|---|
(i) nBuLi, Et2O, (ii) /BRN= 102378/, Et2O, benzene; Multistep reaction; |
2-benzyloxy-5-bromoanisole
homovanillyl alcohol
Conditions | Yield |
---|---|
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
homovanillyl alcohol
Conditions | Yield |
---|---|
With erbium(III) triflate In methanol at 100℃; for 0.75h; Microwave irradiation; |
Conditions | Yield |
---|---|
With methanol; sodium tetrahydroborate In dichloromethane at -78 - 20℃; for 2h; Inert atmosphere; | |
With alcohol dehydrogenase (NC_001145.3) from Saccharomyces cerevisiae S288C |
A
4-n-Propylphenol
B
2-Methoxy-4-methylphenol
C
2-methoxy-4-n-propylphenol
D
2-methoxy-4-propenylphenol
E
4-Ethylguaiacol
F
homovanillyl alcohol
G
4-propylbenzene-1,2-diol
H
benzene-1,2-diol
I
2-methoxy-phenol
J
4-methyl-1,2-dihydroxybenzene
Conditions | Yield |
---|---|
With 5% palladium on Al2O3; hydrogen In water at 25 - 310℃; under 37503.8 Torr; for 1h; Autoclave; |
Conditions | Yield |
---|---|
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
A
2-(3-hydroxy-4-methoxyphenyl)ethanol
B
homovanillyl alcohol
Conditions | Yield |
---|---|
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
2-methoxy-phenol
A
2-(3-hydroxy-4-methoxyphenyl)ethanol
B
homovanillyl alcohol
Conditions | Yield |
---|---|
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
A
2-(3-hydroxy-4-methoxyphenyl)ethanol
B
homovanillyl alcohol
Conditions | Yield |
---|---|
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
A
2-(3-hydroxy-4-methoxyphenyl)ethanol
B
homovanillyl alcohol
Conditions | Yield |
---|---|
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
A
2-(3-hydroxy-4-methoxyphenyl)ethanol
B
homovanillyl alcohol
Conditions | Yield |
---|---|
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 |
A
3,4-dimethoxyphenol
B
4-allylguaiacol
C
1,3-dimethoxy-2-hydroxy-benzene
D
2-Methoxy-4-methylphenol
E
2-methoxy-4-n-propylphenol
F
3-methocycatechol
G
1,2,3-trimethoxybenzene
H
2,4,6-trihydroxyacetophenone
I
4-allyl-2,6-dimethoxyphenol
J
1-(4-hydroxy-3,5-dimethoxy-phenyl)-ethanone
K
3-methoxy-4-hydroxystyrene
L
4-Ethylguaiacol
M
1-(4-hydroxy-3-methoxyphenyl)2-propanone
N
1-(2,4,6-trihydroxy-3-methylphenyl)butan-1-one
O
3-hydroxy-5-tert-butyl-catechol
P
homovanillyl alcohol
Q
benzene-1,2-diol
R
2-methoxy-phenol
S
4-methyl-1,2-dihydroxybenzene
T
syringic aldehyde
U
phenol
Conditions | Yield |
---|---|
at 500℃; for 0.00555556h; Pyrolysis; |
A
4-allylguaiacol
B
1,3-dimethoxy-2-hydroxy-benzene
C
2-Methoxy-4-methylphenol
D
2-methoxy-4-n-propylphenol
E
2,3-Dimethylphenol
F
3-methocycatechol
G
1,2,3-trimethoxybenzene
H
2,6-dihydroxy-4-methoxy-acetophenone
I
4-allyl-2,6-dimethoxyphenol
J
1-(4-hydroxy-3,5-dimethoxy-phenyl)-ethanone
K
3-methoxy-4-hydroxystyrene
L
4-Ethylguaiacol
M
1-(4-hydroxy-3-methoxyphenyl)2-propanone
N
homovanillyl alcohol
O
benzene-1,2-diol
P
2-methoxy-phenol
Q
syringic aldehyde
R
phenol
Conditions | Yield |
---|---|
at 500℃; for 0.00555556h; Pyrolysis; |
p-hydroxyphenethyl alcohol
A
2-(4'-hydroxy-3'-methoxyphenyl)ethyl methyl carbonate
B
homovanillyl alcohol
Conditions | Yield |
---|---|
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
3-bromo-4-hydroxyphenylethyl alcohol
homovanillyl alcohol
Conditions | Yield |
---|---|
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
3-bromo-4-hydroxyphenylethyl alcohol
A
2-(4'-hydroxy-3'-methoxyphenyl)ethyl methyl carbonate
B
homovanillyl alcohol
Conditions | Yield |
---|---|
With sodium methylate; copper(I) bromide In methanol at 100℃; for 15h; |
1-(3,4-dimethoxyphenyl)-5-hydroxydecan-3-one
A
homovanillyl alcohol
E
2-(3,4-dimethoxyphenyl)ethyl alcohol
Conditions | Yield |
---|---|
With Colletotrichum gloeosporioides In water; dimethyl sulfoxide at 30℃; for 120h; Microbiological reaction; |
homovanillyl alcohol
acetic anhydride
4-(2-acetoxyethyl)-2-methoxy-1-acetoxy-benzene
Conditions | Yield |
---|---|
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 pyridine | 95% |
With acetic acid at 50℃; for 12h; | 67% |
homovanillyl alcohol
carbonic acid dimethyl ester
2-(4'-hydroxy-3'-methoxyphenyl)ethyl methyl carbonate
Conditions | Yield |
---|---|
With sulfuric acid for 7h; Reflux; | 100% |
With 1,8-diazabicyclo[5.4.0]undec-7-ene at 90℃; for 7.5h; | 98% |
Conditions | Yield |
---|---|
With triethylamine In N,N-dimethyl-formamide at 20℃; for 3h; | 100% |
With 1H-imidazole |
Conditions | Yield |
---|---|
In carbonic acid dimethyl ester at 20℃; for 24h; | 100% |
Conditions | Yield |
---|---|
With Candida antarctica lipase In various solvent(s) at 40℃; for 1.5h; | 98.1% |
Conditions | Yield |
---|---|
With Candida antarctica lipase In various solvent(s) at 40℃; for 4h; | 98% |
Conditions | Yield |
---|---|
With sulfuric acid at 20℃; | 98% |
Conditions | Yield |
---|---|
With Candida antarctica lipase In various solvent(s) at 40℃; for 1.5h; | 97.5% |
homovanillyl alcohol
hydroxytyrosol
Conditions | Yield |
---|---|
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% |
Conditions | Yield |
---|---|
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% |
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile for 7h; Reflux; | 95% |
8-methylnonanoic acid
homovanillyl alcohol
8-methylnonanoic acid 2-(4-hydroxy-3-methoxyphenyl)ethyl ester
Conditions | Yield |
---|---|
novozyme 435 at 50℃; for 16h; Enzymatic reaction; Neat (no solvent); | 93.2% |
Conditions | Yield |
---|---|
With potassium carbonate In acetone Reflux; | 93% |
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl-formamide for 0.5h; | 93% |
di-tert-butyl dicarbonate
homovanillyl alcohol
Conditions | Yield |
---|---|
With mesoporous silica MCM-41 supported erbium(III) at 40℃; for 9h; Neat (no solvent); ultrasound irradiation; Inert atmosphere; | 92% |
Conditions | Yield |
---|---|
With Candida antarctica lipase In various solvent(s) at 40℃; for 1.5h; | 90.9% |
Conditions | Yield |
---|---|
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% |
About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia
Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog
©2008 LookChem.com,License: ICP
NO.:Zhejiang16009103
complaints:service@lookchem.com Desktop View