875-74-1

  • Product Name:D-2-Phenylglycine
  • Molecular Formula:C8H9NO2
  • Purity:99%
  • Molecular Weight:151.165
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Product Details

Quality Factory Sells Top Purity 99% D-2-Phenylglycine 875-74-1 with Safe Delivery

  • Molecular Formula:C8H9NO2
  • Molecular Weight:151.165
  • Appearance/Colour:white crystalline powder 
  • Vapor Pressure:0.00107mmHg at 25°C 
  • Melting Point:302 °C (dec.)(lit.) 
  • Refractive Index:-158 ° (C=1, 1mol/L HCl) 
  • Boiling Point:288.7 °C at 760 mmHg 
  • PKA:1.94±0.10(Predicted) 
  • Flash Point:128.4 °C 
  • PSA:63.32000 
  • Density:1.246 g/cm3 
  • LogP:1.47130 

D-2-Phenylglycine(Cas 875-74-1) Usage

Storage

Store at room temperature. Store in cool dry place in tightly closed container. Store away from oxidizing agent.

Flammability and Explosibility

Nonflammable

Definition

ChEBI: The R stereoisomer of alpha-phenylglycine.

InChI:InChI=1/C8H9NO2/c9-7(8(10)11)6-4-2-1-3-5-6/h1-5,7H,9H2,(H,10,11)/t7-/m1/s1

875-74-1 Relevant articles

Formation of Quasi-racemic Diastereoisomeric Salts as a Structural Cause for Efficient Optical Resolution

Fogassy, Elemer,Kozma, David

, p. 5069 - 5070 (1995)

During optical resolutions, when the res...

-

Timmermans,Motiuk

, p. 399,408, 410 (1932)

-

The Methyl Ester of α-Aminophenylacetic Acid: pH-Dependence and Phosphate Catalysis of Hydrolysis

Blinkovsky, Alexander M.,Galaev, Igor Yu.,Svedas, Vytas K.

, p. 1537 - 1540 (1986)

The dependence of the rate of spontaneou...

Highly Stable Zr(IV)-Based Metal-Organic Frameworks for Chiral Separation in Reversed-Phase Liquid Chromatography

Jiang, Hong,Yang, Kuiwei,Zhao, Xiangxiang,Zhang, Wenqiang,Liu, Yan,Jiang, Jianwen,Cui, Yong

supporting information, p. 390 - 398 (2021/01/13)

Separation of racemic mixtures is of gre...

D-Phenylglycine aminotransferase (d-PhgAT)-substrate scope and structural insights of a stereo-inverting biocatalyst used in the preparation of aromatic amino acids

Akhtar, M. Kalim,Campopiano, Dominic J.,De Cesare, Silvia,Loake, Gary J.,Marles-Wright, Jon,Serpico, Annabel

, p. 6533 - 6543 (2020/11/13)

Enantiopure amines are key building bloc...

Ultrasound-Controlled Chiral Separation of Four Amino Acids and 2,2,2-Trifluoro-1-(9-anthryl)ethanol

Lee, Jae Hwan,Ryoo, Jae Jeong

, p. 146 - 149 (2019/02/07)

Chiral separation of 4-hydroxyphenylglyc...

Deracemization and stereoinversion to aromatic d-amino acid derivatives with ancestral l-amino acid oxidase

Nakano, Shogo,Minamino, Yuki,Hasebe, Fumihito,Ito, Sohei

, p. 10152 - 10158 (2019/10/19)

Enantiomerically pure amino acid derivat...

875-74-1 Process route

phenylglycin
2835-06-5

phenylglycin

(R)-phenylglycine
875-74-1

(R)-phenylglycine

Benzoylformic acid
611-73-4

Benzoylformic acid

benzoic acid
65-85-0,8013-63-6

benzoic acid

Conditions
Conditions Yield
phenylglycine methyl ester
24461-61-8,26682-99-5,37760-98-8,6591-61-3

phenylglycine methyl ester

(R)-Phenylglycine methyl ester
24461-61-8

(R)-Phenylglycine methyl ester

(S)-2-phenylglycine
2935-35-5

(S)-2-phenylglycine

(R)-phenylglycine
875-74-1

(R)-phenylglycine

(S)-Phenylglycine methyl ester
6591-61-3,24461-61-8,26682-99-5,37760-98-8

(S)-Phenylglycine methyl ester

Conditions
Conditions Yield
With Bacillus licheniformis; sodium hydrogencarbonate; 1-ethyl-3-methylimidazolium acetate; In water; water-d2; at 30 ℃; for 24h;

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