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Dayang Chem (Hangzhou) Co.,Ltd.

As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem's R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis ch

D(+)-Phenylalaninol Manufacturer/High quality/Best price/In stock

Cas:5267-64-1

Min.Order:1 Kilogram

FOB Price: $3.0

Type:Lab/Research institutions

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Hangzhou Dingyan Chem Co., Ltd

------ Items Standard Result Appearance White powder White powder Specific rotation +21.0

High purity 5267-64-1 D(+)-Phenylalaninol

Cas:5267-64-1

Min.Order:1 Gram

FOB Price: $100.0 / 500.0

Type:Trading Company

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Simagchem Corporation

Welcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our

High quality D-2-Phenylalaninol supplier in China

Cas:5267-64-1

Min.Order:0 Metric Ton

Negotiable

Type:Manufacturers

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Wuhan Fortuna Chemical Co.,Ltd

Unique advantages of D(+)-Phenylalaninol Cas 5267-64-1 Guaranteed purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:White to pale yellow crystalline powder Storage:cool dry place Package:1kg/foi

Manufacturer high quality D(+)-Phenylalaninol Cas 5267-64-1 with good price

Cas:5267-64-1

Min.Order:1 Kilogram

Negotiable

Type:Trading Company

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Ality Chemical Corporation

The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi

Factory Supply (R)-2-amino-3-phenylpropanol

Cas:5267-64-1

Min.Order:1

Negotiable

Type:Other

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Chengdu Baishixing Science and Technology Industry Co., Ltd.

The area of Chengdu Baishixing is 35,000 square metre , the staff members are 88, our output value is over 120 millions per year. Baishiying cooporates with Life Science Academy of Wuhan University to develop amino acids series products.We have profe

D(+)-Phenylalaninol

Cas:5267-64-1

Min.Order:25 Kilogram

FOB Price: $1.0

Type:Manufacturers

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Chemwill Asia Co., Ltd.

Our main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block

D-Phenylalaninol

Cas:5267-64-1

Min.Order:5 Kiloliter

FOB Price: $1.2 / 5.0

Type:Manufacturers

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Hubei DiBo chemical co., LTD

Name: S/R-phenylalanine Name: D-(+) -2-Amino-3-phenyl-1-propanol Chinese aliases: D - (+) - phenylalanine alcohol; D - (+) - 2 - amino - 3 - phenyl - 1 - propanol; D - phenylalanine alcohol CAS No. 5267-64-1 Molecular formula: C9

D-(+)-2-Amino-3-phenyl-1-propanol

Cas:5267-64-1

Min.Order:25 Kilogram

FOB Price: $1.0 / 2.0

Type:Other

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Hebei Nengqian Chemical Import and Export Co., LTD

Our advantages: 1. All inquiries will be replied within 12 hours. 2. Dedication to quality, supply & service. 3. Strictly on selecting raw materials. 4. Reasonable & competitive price, fast lead time. 5. Sample is available for your eva

Factory Supply D(+)-Phenylalaninol

Cas:5267-64-1

Min.Order:1 Kilogram

FOB Price: $9.0 / 99.0

Type:Trading Company

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LIDE PHARMACEUTICALS LIMITED

Advantage : LIDE PHARMACEUTICALS LTD. is a mid-small manufacturing-type enterprise, engaged in pharmaceutical intermediates of R&D, custom-made and production, and also involving trading chemicals for export. We have established the R&amp

D(+)-Phenylalaninol/ LIDE PHARMA- Factory supply / Best price

Cas:5267-64-1

Min.Order:0

Negotiable

Type:Lab/Research institutions

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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 ♦ W

D(+)-PhenylalaninolCAS:5267-64-1

Cas:5267-64-1

Min.Order:1 Kilogram

FOB Price: $20.0 / 30.0

Type:Trading Company

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Shanghai Upbio Tech Co.,Ltd

1.No Less 8 years exporting experience. Clients 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 Specialized

D(+)-Phenylalaninol 5267-64-1

Cas:5267-64-1

Min.Order:1 Kilogram

Negotiable

Type:Lab/Research institutions

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Baoji Guokang Healthchem co.,ltd

Our company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad. At prese

D(+)-Phenylalaninol 99%

Cas:5267-64-1

Min.Order:1 Kilogram

FOB Price: $294.0 / 314.0

Type:Trading Company

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Qingdao Beluga Import and Export Co., LTD

D(+)-Phenylalaninol CAS:5267-64-1 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 interm

D(+)-Phenylalaninol CAS:5267-64-1

Cas:5267-64-1

Min.Order:1 Gram

Negotiable

Type:Lab/Research institutions

inquiry

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

D(+)-Phenylalaninol

Cas:5267-64-1

Min.Order:0

Negotiable

Type:Lab/Research institutions

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Xiamen Hisunny Chemical Co.,Ltd

Best quality & Attractive price & Professional service; Trial & Pilot & Commercial Hisunny Chemical is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality intermediates, specia

D-2-Phenylalaninol

Cas:5267-64-1

Min.Order:0

Negotiable

Type:Manufacturers

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Afine Chemicals Limited

Company Introduction 1. Established in 2005, with two independent business divisions: Fine chemicals division; Pharmaceutical division. 2. Main product: Optical brightener Textile auxiliary Dye stuff Pigments

D(+)-PHENYLALANINOL

Cas:5267-64-1

Min.Order:1 Gram

Negotiable

Type:Lab/Research institutions

inquiry

Hangzhou Keyingchem Co.,Ltd

Hangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det

S/R-phenylalaninol

Cas:5267-64-1

Min.Order:0 Metric Ton

Negotiable

Type:Lab/Research institutions

inquiry

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

D(+)-Phenylalaninol

Cas:5267-64-1

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Hangzhou Lingrui Chemical Co.,Ltd.

our strengths: 1: Fast and guaranteed shipment (TNT;EMS;FEDEX;DHL;UPS;EUB, special line) 2: Various payment items accepted (Btc; MoneyGram; WU) 3: Valued package (Paraffin coating; Double aluminum foil bag; Vacuum packaging) 4: Efficient delivery

Factory Supply D(+)-Phenylalaninol

Cas:5267-64-1

Min.Order:1 Gram

Negotiable

Type:Other

inquiry

Shanghai Massive Chemical Technology Co., Ltd.

Massive Chemical is certified with ISO9001 and ISO14001 manufacturer for this product. We will offer all documents as requirement for the materials which includes, Certificate of Analysis, Material Safety Data Sheet, and Method of Analysis and

D(+)-Phenylalaninol

Cas:5267-64-1

Min.Order:1 Gram

FOB Price: $1.0

Type:Lab/Research institutions

inquiry

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

High quality D-2-Phenylalaninol

Cas:5267-64-1

Min.Order:10 Gram

FOB Price: $100.0

Type:Lab/Research institutions

inquiry

Henan Tianfu Chemical Co., Ltd.

Product Name: D(+)-Phenylalaninol Synonyms: D-(+)-Phenylalinol;S/R-Phenylalaninol;(2R)-2-amino-3-phenylpropan-1-ol;BENZENEPROPANOL, .BETA.-AMINO-, (.BETA.R)-;D-Penylalaninol;D-PHEYLALANINOL;D-PHENYLANINOL;(D)-(+)-2-PHENYLALANINOL / D-(+)-2-AMINO-3

5267-64-1 D(+)-Phenylalaninol

Cas:5267-64-1

Min.Order:1 Kilogram

FOB Price: $500.0

Type:Lab/Research institutions

inquiry

Enke Pharma-tech Co.,Ltd. (Cangzhou, China )

Cangzhou Enke Pharma Tech Co.,ltd. is located in Cangzhou City, Hebei province ,where is a famous petroleum chemical industry city in China. Enke Pharma a high-tech enterprise ,and we are dedicated to developing and manufacturing new api, in

D(+)-Phenylalaninol

Cas:5267-64-1

Min.Order:1 Kilogram

FOB Price: $350.0 / 400.0

Type:Lab/Research institutions

inquiry

Hubei Vanz Pharm Co.,Ltd

D Phenylalaninol powder cas 5267-64-1 Product Name China Manufacturer Supply D(+)-Phenylalaninol CAS 5267-64-1 CAS NO. 5267-64-1 Appearance White Powder

D Phenylalaninol powder cas 5267-64-1

Cas:5267-64-1

Min.Order:1 Kilogram

Negotiable

Type:Trading Company

inquiry

Xiamen Jenny Chemical Technology Co., Ltd.

GMP standard, high purity, competitive price, in stock 1. Quick Response: within 6 hours after receiving your email. 2. Quality Guarantee: All products are strictly tested by our QC, confirmed by QA, and approved by a third-party lab in China, USA,

D(+)-Phenylalaninol

Cas:5267-64-1

Min.Order:1 Milligram

Negotiable

Type:Trading Company

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Henan Kanbei Chemical Co.,LTD

High quality, competitive price, fast delivery and first-class service we possesses have won the trust and praise of customers. Standard: BP/USP/EP The purity is equal or greater than 99%. As a supplier, we can provide high-quality products. Cle

D-Phenylalaninol;(R)-2-Amino-3-phenyl-1-propanol;D(+)-Phenylalaninol;D(+)-2-Amino-3-phenyl-1-propanol.99%

Cas:5267-64-1

Min.Order:1 Metric Ton

Negotiable

Type:Lab/Research institutions

inquiry

Shanghai Minstar Chemical Co., Ltd

D(+)-Phenylalaninol Chemical Properties Melting point 93-95 °C(lit.) alpha 23 º (c=1.2, 1 N HCl 22 ºC) Boiling point 122 °C / 4mmHg density 1.0406 (rough estimate) refractive index 23.5 ° (C=1.2, 1mol/L HCl)

D-Phenylalaninol

Cas:5267-64-1

Min.Order:1 Gram

FOB Price: $66.0

Type:Lab/Research institutions

inquiry

Siwei Development Group Ltd.

Product name: D-Phenylalaninol CAS No.: 5267-64-1 Molecule Formula:C9H13NO Molecule Weight:151.21 Purity: 99.0% Package: 25kg/drum Description:White to off-white crystalline powder Manufacture Standards:Enterprise Standard

Lower Price D-Phenylalaninol

Cas:5267-64-1

Min.Order:1 Kilogram

Negotiable

Type:Trading Company

inquiry

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

BEST PRICE/D(+)-Phenylalaninol CAS NO.5267-64-1

Cas:5267-64-1

Min.Order:1 Metric Ton

FOB Price: $7.0 / 8.0

Type:Trading Company

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Synthetic route

D-(R)-phenylalanine
673-06-3

D-(R)-phenylalanine

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With lithium borohydride; chloro-trimethyl-silane In tetrahydrofuran at 20℃; for 0.25h; Reduction;99%
With sodium tetrahydroborate; iodine In tetrahydrofuran at 0℃; Reflux;99%
With sodium tetrahydroborate; sulfuric acid In tetrahydrofuran at 20℃;98%
(R)-N-(1-hydroxy-3-phenylpropan-2-yl)acetamide

(R)-N-(1-hydroxy-3-phenylpropan-2-yl)acetamide

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With sulfuric acid In water at 120℃;98%
With sulfuric acid at 100℃; for 48h; Darkness;143.7 mg
(R)-2-amino-3-phenylpropionitrile hydrochloride

(R)-2-amino-3-phenylpropionitrile hydrochloride

A

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

B

(R)-3-phenylpropane-1,2-diamine
85612-59-5

(R)-3-phenylpropane-1,2-diamine

Conditions
ConditionsYield
With hydrogenchloride; methanol; water; hydrogen; 5% palladium over charcoal at 35℃; under 6750.68 - 22502.3 Torr; for 43h;A 91%
B 6%
(R)-4-(phenylmethyl)-2-oxazolidinone
40217-17-2, 90719-32-7, 120574-96-1, 102029-44-7

(R)-4-(phenylmethyl)-2-oxazolidinone

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With ammonium bromide; 3-azapentane-1,5-diamine at 90℃; for 5h; Microwave irradiation;84%
9H-fluoren-9-ylmethyl (R)-<1-(hydroxymethyl)-2-phenylethyl>carbamate
130406-30-3

9H-fluoren-9-ylmethyl (R)-<1-(hydroxymethyl)-2-phenylethyl>carbamate

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With piperidine In dichloromethane for 1h; Ambient temperature;82%
D-phenylalanine methyl ester
21685-51-8

D-phenylalanine methyl ester

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With methanol; sodium tetrahydroborate at 0 - 10℃; for 1h; Temperature; Solvent;81%
(1R,1'R)-N,1'-dibenzyl-1-phenyl-2,2'-dihydroxydiethylamine

(1R,1'R)-N,1'-dibenzyl-1-phenyl-2,2'-dihydroxydiethylamine

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With ammonium formate; palladium on activated charcoal In methanol for 2h; Heating;80%
(+)-(R)-2-(1-benzyl-2-hydroxyethyl)-1H-isoindole-1,3(2H)-dione
152903-44-1

(+)-(R)-2-(1-benzyl-2-hydroxyethyl)-1H-isoindole-1,3(2H)-dione

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With hydrazine hydrate In acetonitrile for 4h; Heating;73%
(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
Stage #1: rac-phenylalaninol With O,O'-dibenzoyl-L-tartaric acid In acetone at 25℃; for 6h;
Stage #2: With potassium hydroxide In dichloromethane
52%
(L)-phenylalanine ethyl ester hydrochloride
3182-93-2

(L)-phenylalanine ethyl ester hydrochloride

A

L-Phenylalaninol
3182-95-4

L-Phenylalaninol

B

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With methanol; Na/SiO2 In tetrahydrofuran at 0 - 25℃; Bouveault-Blanc reduction; Inert atmosphere; optical yield given as %ee;A 27%
B n/a
D-phenylalanine ethyl ester
1795-96-6, 3081-24-1, 20529-91-3

D-phenylalanine ethyl ester

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With lithium aluminium tetrahydride In diethyl ether
methyl (2S)-2-amino-3-phenylpropanoate
2577-90-4

methyl (2S)-2-amino-3-phenylpropanoate

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With lithium aluminium tetrahydride In tetrahydrofuran

A

L-Phenylalaninol
3182-95-4

L-Phenylalaninol

B

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

C

(R)-Mandelic Acid
611-71-2

(R)-Mandelic Acid

D

(R)-N-<(S)-1-benzyl-2-hydroxyethyl>mandelamide
113336-57-5

(R)-N-<(S)-1-benzyl-2-hydroxyethyl>mandelamide

Conditions
ConditionsYield
With Alcaligenes PA In water at 25℃; pH=10;
ethyl 2-(hydroxyimino)-3-phenylpropanoate
6943-96-0, 70564-52-2, 70564-53-3

ethyl 2-(hydroxyimino)-3-phenylpropanoate

A

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

B

O=CH(CH2)2NHCOO-Wang-polystyrene

O=CH(CH2)2NHCOO-Wang-polystyrene

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: 80 percent / NaBH4; I2 / tetrahydrofuran / 4 h / Heating
2.1: dibenzoyl-L-tartaric acid / acetone / 6 h / 25 °C
2.2: 52 percent / aq. KOH / CH2Cl2
View Scheme
Boc-D-Phe-OH
18942-49-9

Boc-D-Phe-OH

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: BH3*THF
2: H3O(1+)
View Scheme
Hydroxymethyl-((R)-1-hydroxymethyl-2-phenyl-ethyl)-carbamic acid tert-butyl ester
210561-40-3

Hydroxymethyl-((R)-1-hydroxymethyl-2-phenyl-ethyl)-carbamic acid tert-butyl ester

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 82 percent / NaOH / methanol; H2O / Ambient temperature
2: H3O(1+)
View Scheme
(1S,2S)-2-amino-1-phenyl-1,3-diol
28143-91-1

(1S,2S)-2-amino-1-phenyl-1,3-diol

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: 93 percent / xylene / 2 h / Heating
2: 1.) SOCl2, 2.) LiBr / 1.) CHCl3, 8 h, 2.) Me2CO, 6 h
3: 80 percent / LiAlH4 / tetrahydrofuran / 2 h / Heating
4: 73 percent / NH2NH2*H2O / acetonitrile / 4 h / Heating
View Scheme
Multi-step reaction with 5 steps
1: 93 percent / xylene / 2 h / Heating
2: 60 percent / SOCl2, Et3N / CH2Cl2 / 1 h / 0 °C
3: 60 percent / LiBr, PTSA / acetonitrile / 2 h / Ambient temperature
4: 80 percent / LiAlH4 / tetrahydrofuran / 2 h / Heating
5: 73 percent / NH2NH2*H2O / acetonitrile / 4 h / Heating
View Scheme
(1S,2S)-1-phenyl-2-phthalimido-propane-1,3-diol
123537-84-8

(1S,2S)-1-phenyl-2-phthalimido-propane-1,3-diol

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 1.) SOCl2, 2.) LiBr / 1.) CHCl3, 8 h, 2.) Me2CO, 6 h
2: 80 percent / LiAlH4 / tetrahydrofuran / 2 h / Heating
3: 73 percent / NH2NH2*H2O / acetonitrile / 4 h / Heating
View Scheme
Multi-step reaction with 4 steps
1: 60 percent / SOCl2, Et3N / CH2Cl2 / 1 h / 0 °C
2: 60 percent / LiBr, PTSA / acetonitrile / 2 h / Ambient temperature
3: 80 percent / LiAlH4 / tetrahydrofuran / 2 h / Heating
4: 73 percent / NH2NH2*H2O / acetonitrile / 4 h / Heating
View Scheme
2-((S)-2-Bromo-1-hydroxymethyl-2-phenyl-ethyl)-isoindole-1,3-dione

2-((S)-2-Bromo-1-hydroxymethyl-2-phenyl-ethyl)-isoindole-1,3-dione

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 80 percent / LiAlH4 / tetrahydrofuran / 2 h / Heating
2: 73 percent / NH2NH2*H2O / acetonitrile / 4 h / Heating
View Scheme
2-((4S,5S)-2-Oxo-4-phenyl-2λ4-[1,3,2]dioxathian-5-yl)-isoindole-1,3-dione
176538-77-5

2-((4S,5S)-2-Oxo-4-phenyl-2λ4-[1,3,2]dioxathian-5-yl)-isoindole-1,3-dione

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 60 percent / LiBr, PTSA / acetonitrile / 2 h / Ambient temperature
2: 80 percent / LiAlH4 / tetrahydrofuran / 2 h / Heating
3: 73 percent / NH2NH2*H2O / acetonitrile / 4 h / Heating
View Scheme
(4R,4R)-N,2-dibenzyl-4-phenyl-1,3-oxazolidine

(4R,4R)-N,2-dibenzyl-4-phenyl-1,3-oxazolidine

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 2.) KF, NaHCO3, 30percent H2O2 / 1.) THF, RT, 24 h, 2.) THF, methanol, RT, 48 h
2: 80 percent / HCO2NH4 / 10percent Pd-C / methanol / 2 h / Heating
View Scheme
(-)-(R)-(N-9-fluorenylmethoxycarbonyl)phenylalaninal
146803-47-6

(-)-(R)-(N-9-fluorenylmethoxycarbonyl)phenylalaninal

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 95 percent / sodium borohydride / tetrahydrofuran / 2 h / 0 °C
2: 82 percent / piperidine / CH2Cl2 / 1 h / Ambient temperature
View Scheme
(R)-dibenzyl 1-(1-hydroxy-3-phenylpropan-2-yl)hydrazine-1,2-dicarboxylate
438470-79-2

(R)-dibenzyl 1-(1-hydroxy-3-phenylpropan-2-yl)hydrazine-1,2-dicarboxylate

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With hydrogen; nickel In methanol; acetic acid at 25℃; under 3102.97 Torr; for 20h;
(R)-2-nitro-3-phenylpropan-1-ol
1255037-12-7

(R)-2-nitro-3-phenylpropan-1-ol

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With sulfuric acid; zinc In water

A

L-Phenylalaninol
3182-95-4

L-Phenylalaninol

B

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With chiral stationary phase including isopropyl-functionalized CF6 In methanol; acetic acid; triethylamine; acetonitrile at 20℃; Purification / work up;
With C45H31O4P In aq. phosphate buffer; chloroform at 6℃; for 16h; Reagent/catalyst; Sealed tube; Resolution of racemate;
With (S)-(+)-3,3'-diphenyl-2,2'-bi-1-naphthol hydrogen phosphate In aq. phosphate buffer; chloroform; water at 6℃; for 16h; pH=5; Reagent/catalyst; enantioselective reaction;A n/a
B n/a
α-Acetamido-cinnamaldehyd
3548-71-8

α-Acetamido-cinnamaldehyd

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: (R,R)-(-)-2,3-bis(tert-butylmethylphosphino)benzene; di[(η-1,2,5,6)-1,5-cyclooctadiene] rhodium hexafluoroantimonate; hydrogen / dichloromethane / 12 h / 20 °C / Autoclave
2: sulfuric acid / 48 h / 100 °C / Darkness
View Scheme
Multi-step reaction with 2 steps
1: di[(η-1,2,5,6)-1,5-cyclooctadiene] rhodium hexafluoroantimonate; hydrogen; (R)-1-[(Sp)-2-(diphenylphosphino)ferrocenyl]ethyldicyclohexylphosphine / dichloromethane / 4 h / 20 °C / 22801.5 Torr / Autoclave
2: sulfuric acid / 48 h / 100 °C / Darkness
View Scheme
Multi-step reaction with 3 steps
1: (R,R)-(-)-2,3-bis(tert-butylmethylphosphino)benzene; di[(η-1,2,5,6)-1,5-cyclooctadiene] rhodium hexafluoroantimonate; hydrogen / ethyl acetate / 4 h / 20 °C / 22801.5 Torr / Autoclave
2: sodium tetrahydroborate
3: sulfuric acid / 48 h / 100 °C / Darkness
View Scheme
Multi-step reaction with 3 steps
1: (R,R)-(-)-2,3-bis(tert-butylmethylphosphino)benzene; di[(η-1,2,5,6)-1,5-cyclooctadiene] rhodium hexafluoroantimonate; hydrogen / dichloromethane / 4 h / 20 °C / Autoclave
2: sodium tetrahydroborate
3: sulfuric acid / 48 h / 100 °C / Darkness
View Scheme
Multi-step reaction with 3 steps
1: di[(η-1,2,5,6)-1,5-cyclooctadiene] rhodium hexafluoroantimonate; hydrogen; (R)-1-[(Sp)-2-(diphenylphosphino)ferrocenyl]ethyldicyclohexylphosphine / dichloromethane / 4 h / 20 °C / 22801.5 Torr / Autoclave
2: sodium tetrahydroborate
3: sulfuric acid / 48 h / 100 °C / Darkness
View Scheme
(R)-N-(1-oxo-3-phenylpropan-2-yl)acetamide

(R)-N-(1-oxo-3-phenylpropan-2-yl)acetamide

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: sodium tetrahydroborate
2: sulfuric acid / 48 h / 100 °C / Darkness
View Scheme
di-tert-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

N-tert-butoxycarbonyl-D-Phenylalaninol
106454-69-7

N-tert-butoxycarbonyl-D-Phenylalaninol

Conditions
ConditionsYield
In dichloromethane at 0 - 20℃;100%
In ethanol at 30℃; for 0.0166667h;99%
In chloroform at 0 - 20℃; Substitution;95%
(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

chloroacetyl chloride
79-04-9

chloroacetyl chloride

2-chloro-N-(1-hydroxymethyl-2-phenyl-ethyl)-acetamide
466695-52-3

2-chloro-N-(1-hydroxymethyl-2-phenyl-ethyl)-acetamide

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 25℃;100%
tert-butyldicarbonate
34619-03-9

tert-butyldicarbonate

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

N-tert-butoxycarbonyl-D-Phenylalaninol
106454-69-7

N-tert-butoxycarbonyl-D-Phenylalaninol

Conditions
ConditionsYield
With sodium hydroxide In dichloromethane; water at 20℃; for 24h;100%
(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

1-chloro-2(R)-amino-phenylpropane hydrochloride
100431-27-4

1-chloro-2(R)-amino-phenylpropane hydrochloride

Conditions
ConditionsYield
With thionyl chloride In N,N-dimethyl-formamide at 120℃; for 2h;99%
(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

methyl chloroformate
79-22-1

methyl chloroformate

R-(+)-N,O-bis(methoxycarbonyl)-2-amino-3-phenylpropanol
252659-50-0

R-(+)-N,O-bis(methoxycarbonyl)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With pyridine In chloroform at 20℃; for 14h; Condensation;99%
(R)-(-)-1,1',6,6',7,7'-hexahydroxy-5,5'-diisopropyl-3,3'-dimethyl-2,2'-binaphthyl-8,8'-dicarbaldehyde

(R)-(-)-1,1',6,6',7,7'-hexahydroxy-5,5'-diisopropyl-3,3'-dimethyl-2,2'-binaphthyl-8,8'-dicarbaldehyde

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

C48H52N2O8

C48H52N2O8

Conditions
ConditionsYield
In methanol at 20℃; for 3h; Inert atmosphere; optical yield given as %de;99%
(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

4-bromobenzenesulfonyl chloride
98-58-8

4-bromobenzenesulfonyl chloride

(R)-4-bromo-N-(1-hydroxy-3-phenylpropan-2-yl)benzenesulfonamide

(R)-4-bromo-N-(1-hydroxy-3-phenylpropan-2-yl)benzenesulfonamide

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃; for 1h;99%
(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

2,2-Dimethylmalonyl chloride
5659-93-8

2,2-Dimethylmalonyl chloride

(R,R)-N,N'-bis(1-benzyl-2-hydroxyethyl)-2,2-dimethylpropane-1,3-diamide

(R,R)-N,N'-bis(1-benzyl-2-hydroxyethyl)-2,2-dimethylpropane-1,3-diamide

Conditions
ConditionsYield
With triethylamine In dichloromethane 0 deg C, 30 min; 23 deg C, 2 h;97%
carbon dioxide
124-38-9

carbon dioxide

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

(R)-4-(phenylmethyl)-2-oxazolidinone
40217-17-2, 90719-32-7, 120574-96-1, 102029-44-7

(R)-4-(phenylmethyl)-2-oxazolidinone

Conditions
ConditionsYield
With triethylamine; chlorophosphoric acid diphenyl ester In acetonitrile at -40 - 25℃;97%
Stage #1: carbon dioxide; (R)-2-amino-3-phenylpropanol With 1,8-diazabicyclo[5.4.0]undec-7-ene In acetonitrile at 20℃; for 0.75h;
Stage #2: With tributylphosphine; di-tert-butyl-diazodicarboxylate In acetonitrile at 0℃; for 0.333333h; Mitsunobu reaction;
78%
With tetramethylphenylguanidine; diphenyl phosphoryl azide In acetonitrile at -40 - 20℃;75%
phthalic anhydride
85-44-9

phthalic anhydride

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

(+)-(R)-2-(1-benzyl-2-hydroxyethyl)-1H-isoindole-1,3(2H)-dione
152903-44-1

(+)-(R)-2-(1-benzyl-2-hydroxyethyl)-1H-isoindole-1,3(2H)-dione

Conditions
ConditionsYield
at 140℃;96%
With triethylamine In toluene for 3h; Condensation; Heating;93%
at 200℃; for 3h;91%
at 140 - 150℃; for 6h;82%
(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

6-methoxy-4-((1R)-methoxy((1S,4S,5R)-5-vinylquinuclidin-2-yl)methyl)quinoline-2-carboxyli c acid

6-methoxy-4-((1R)-methoxy((1S,4S,5R)-5-vinylquinuclidin-2-yl)methyl)quinoline-2-carboxyli c acid

N-((R)-1-hydroxy-3-phenylpropan-2-yl)-6-methoxy-4-((1R)-methoxy((1S,4S,5R)-5-vinylquin uclidin-2-yl)methyl)quinoline-2-carboxamide

N-((R)-1-hydroxy-3-phenylpropan-2-yl)-6-methoxy-4-((1R)-methoxy((1S,4S,5R)-5-vinylquin uclidin-2-yl)methyl)quinoline-2-carboxamide

Conditions
ConditionsYield
With 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane Cooling with ice;96%
(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

4,6-dichloro-1-phenyl-1H-pyrazolo<3,4-d>pyrimidine
99971-84-3

4,6-dichloro-1-phenyl-1H-pyrazolo<3,4-d>pyrimidine

(R)-β-<(1-phenyl-6-chloro-1H-pyrazolo<3,4-d>pyrimidin-4-yl)amino>benzenepropanol
132537-83-8

(R)-β-<(1-phenyl-6-chloro-1H-pyrazolo<3,4-d>pyrimidin-4-yl)amino>benzenepropanol

Conditions
ConditionsYield
In ethanol for 48h; Ambient temperature;95%
In ethanol95%
(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

benzoyl chloride
98-88-4

benzoyl chloride

N-benzoyl-D-phenylalaninol
5267-65-2

N-benzoyl-D-phenylalaninol

Conditions
ConditionsYield
With potassium carbonate In methanol at 20℃;95%
With potassium carbonate In methanol at 20℃;95%
With potassium carbonate In methanol at 20℃;95%
With potassium carbonate In methanol at 20℃; Acylation;
With potassium carbonate In methanol at 20℃;
4-Chloro-2-phenyl-7-propyl-2H-pyrazolo[3,4-d]pyrimidin-6(7H)-one
791071-50-6

4-Chloro-2-phenyl-7-propyl-2H-pyrazolo[3,4-d]pyrimidin-6(7H)-one

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

(R)-4-(1-hydroxy-3-phenylprop-2-ylamino)-2-phenyl-7-propyl-2H-pyrazolo[3,4-d]pyrimidin-6(7H)-one
791071-43-7

(R)-4-(1-hydroxy-3-phenylprop-2-ylamino)-2-phenyl-7-propyl-2H-pyrazolo[3,4-d]pyrimidin-6(7H)-one

Conditions
ConditionsYield
In isopropyl alcohol Heating / reflux;95%
(2-oxocyclopent)acetic acid
104115-44-8

(2-oxocyclopent)acetic acid

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

(3R,5aR,8aS)-3-benzyl-hexahydro-1-oxa-3a-aza-cyclopenta[c]pentalen-4-one
1240492-77-6

(3R,5aR,8aS)-3-benzyl-hexahydro-1-oxa-3a-aza-cyclopenta[c]pentalen-4-one

Conditions
ConditionsYield
at 110℃; under 11251.1 Torr; Meyer synthesis; Microwave irradiation; optical yield given as %de;95%
In water at 100℃; for 16h;80%
(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

(1S,4S,5S,7R)-5-chloro-7-((6-chloro-9H-purin-9-yl)methyl)bicyclo[2.2.1]heptan-2-ol

(1S,4S,5S,7R)-5-chloro-7-((6-chloro-9H-purin-9-yl)methyl)bicyclo[2.2.1]heptan-2-ol

(1S,4S,5S,7R)-5-chloro-7-((6-(((R)-1-hydroxy-3-phenylpropan-2-yl)amino)-9H-purin-9-yl)methyl)bicyclo[2.2.1]heptan-2-ol

(1S,4S,5S,7R)-5-chloro-7-((6-(((R)-1-hydroxy-3-phenylpropan-2-yl)amino)-9H-purin-9-yl)methyl)bicyclo[2.2.1]heptan-2-ol

Conditions
ConditionsYield
With triethylamine In ethanol at 60℃; for 72h;94.1%
(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Boc-Phe-ONSu
3674-06-4

Boc-Phe-ONSu

tert-butyl ((2S)-1-(((2R)-1-hydroxy-3-phenylpropan-2-yl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate
138772-68-6

tert-butyl ((2S)-1-(((2R)-1-hydroxy-3-phenylpropan-2-yl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran Ambient temperature;94%
9-Chloroacridine
1207-69-8

9-Chloroacridine

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

(R)-2-(Acridin-9-ylamino)-3-phenyl-propan-1-ol

(R)-2-(Acridin-9-ylamino)-3-phenyl-propan-1-ol

Conditions
ConditionsYield
In various solvent(s) at 80 - 85℃; for 2h;94%
(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

(S)-(+)-1,1',6,6',7,7'-hexahydroxy-5,5'-diisopropyl-3,3'-dimethyl-2,2'-binaphthyl-8,8'-dicarbaldehyde

(S)-(+)-1,1',6,6',7,7'-hexahydroxy-5,5'-diisopropyl-3,3'-dimethyl-2,2'-binaphthyl-8,8'-dicarbaldehyde

C48H52N2O8

C48H52N2O8

Conditions
ConditionsYield
In methanol at 20℃; for 3h; Inert atmosphere; optical yield given as %de;94%
(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

tert-butyl N-{2-[4-(isothiocyanatomethyl)benzamido]phenyl}carbamate
1448350-40-0

tert-butyl N-{2-[4-(isothiocyanatomethyl)benzamido]phenyl}carbamate

tert-butyl N-(2-{4-[({[(2R)-1-hydroxy-3-phenylpropan-2-yl]carbamothioyl}amino)methyl]benzamido}phenyl)carbamate
1448350-45-5

tert-butyl N-(2-{4-[({[(2R)-1-hydroxy-3-phenylpropan-2-yl]carbamothioyl}amino)methyl]benzamido}phenyl)carbamate

Conditions
ConditionsYield
In acetonitrile at 20℃; for 16h;94%
In tetrahydrofuran at 20℃; for 16h;
(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

1,2-bis(dicyclohexylamino)-3-chlorocyclopropenium chloride

1,2-bis(dicyclohexylamino)-3-chlorocyclopropenium chloride

(R)-2-(2,3-bis(dicyclohexylamino)cyclopropenimine)-3-phenylpropan-1-ol hydrochloride
1620078-17-2

(R)-2-(2,3-bis(dicyclohexylamino)cyclopropenimine)-3-phenylpropan-1-ol hydrochloride

Conditions
ConditionsYield
Stage #1: (R)-2-amino-3-phenylpropanol; 1-chloro-2,3-bis(dicyclohexylamino)cyclopropenium chloride With N-ethyl-N,N-diisopropylamine In dichloromethane at 23℃; for 12h;
Stage #2: With hydrogenchloride In dichloromethane
93%
thiophene-2-carbaldehyde
98-03-3

thiophene-2-carbaldehyde

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

(R)-3-phenyl-2-[(thien-2-ylmethyl)amino]propan-1-ol

(R)-3-phenyl-2-[(thien-2-ylmethyl)amino]propan-1-ol

Conditions
ConditionsYield
Stage #1: thiophene-2-carbaldehyde; (R)-2-amino-3-phenylpropanol In methanol at 20℃;
Stage #2: With sodium tetrahydroborate In ethanol at 0℃; Further stages.;
92%
D-(R)-phenylalanine
673-06-3

D-(R)-phenylalanine

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With lithium borohydride; chloro-trimethyl-silane In tetrahydrofuran at 20℃; for 0.25h; Reduction;99%
With sodium tetrahydroborate; iodine In tetrahydrofuran at 0℃; Reflux;99%
With sodium tetrahydroborate; sulfuric acid In tetrahydrofuran at 20℃;98%
(R)-N-(1-hydroxy-3-phenylpropan-2-yl)acetamide

(R)-N-(1-hydroxy-3-phenylpropan-2-yl)acetamide

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With sulfuric acid In water at 120℃;98%
With sulfuric acid at 100℃; for 48h; Darkness;143.7 mg
(R)-2-amino-3-phenylpropionitrile hydrochloride

(R)-2-amino-3-phenylpropionitrile hydrochloride

A

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

B

(R)-3-phenylpropane-1,2-diamine
85612-59-5

(R)-3-phenylpropane-1,2-diamine

Conditions
ConditionsYield
With hydrogenchloride; methanol; water; hydrogen; 5% palladium over charcoal at 35℃; under 6750.68 - 22502.3 Torr; for 43h;A 91%
B 6%
(R)-4-(phenylmethyl)-2-oxazolidinone
40217-17-2, 90719-32-7, 120574-96-1, 102029-44-7

(R)-4-(phenylmethyl)-2-oxazolidinone

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With ammonium bromide; 3-azapentane-1,5-diamine at 90℃; for 5h; Microwave irradiation;84%
9H-fluoren-9-ylmethyl (R)-<1-(hydroxymethyl)-2-phenylethyl>carbamate
130406-30-3

9H-fluoren-9-ylmethyl (R)-<1-(hydroxymethyl)-2-phenylethyl>carbamate

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With piperidine In dichloromethane for 1h; Ambient temperature;82%
D-phenylalanine methyl ester
21685-51-8

D-phenylalanine methyl ester

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With methanol; sodium tetrahydroborate at 0 - 10℃; for 1h; Temperature; Solvent;81%
(1R,1'R)-N,1'-dibenzyl-1-phenyl-2,2'-dihydroxydiethylamine

(1R,1'R)-N,1'-dibenzyl-1-phenyl-2,2'-dihydroxydiethylamine

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With ammonium formate; palladium on activated charcoal In methanol for 2h; Heating;80%
(+)-(R)-2-(1-benzyl-2-hydroxyethyl)-1H-isoindole-1,3(2H)-dione
152903-44-1

(+)-(R)-2-(1-benzyl-2-hydroxyethyl)-1H-isoindole-1,3(2H)-dione

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With hydrazine hydrate In acetonitrile for 4h; Heating;73%
(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
Stage #1: rac-phenylalaninol With O,O'-dibenzoyl-L-tartaric acid In acetone at 25℃; for 6h;
Stage #2: With potassium hydroxide In dichloromethane
52%
(L)-phenylalanine ethyl ester hydrochloride
3182-93-2

(L)-phenylalanine ethyl ester hydrochloride

A

L-Phenylalaninol
3182-95-4

L-Phenylalaninol

B

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With methanol; Na/SiO2 In tetrahydrofuran at 0 - 25℃; Bouveault-Blanc reduction; Inert atmosphere; optical yield given as %ee;A 27%
B n/a
D-phenylalanine ethyl ester
1795-96-6, 3081-24-1, 20529-91-3

D-phenylalanine ethyl ester

(R)-2-amino-3-phenylpropanol
5267-64-1

(R)-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With lithium aluminium tetrahydride In diethyl ether

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