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P25485

D−(−)-α-Phenylglycine

Name: <SC>D</SC>−(−)-α-Phenylglycine
Brand: ALDRICH

99%, detection

Sinonimo/i:

(R)-(−)-2-Phenylglycine, D-2-Phenylglycine, R-(−)-α-Aminophenylacetic acid

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About This Item

Formula condensata:

C₆H₅CH(NH₂)CO₂H

Numero CAS:

875-74-1

Peso molecolare:

151.16

Beilstein:

2208676

Numero CE:

212-876-3

Numero MDL:

MFCD00008061

Codice UNSPSC:

12352209

ID PubChem:

24898336

NACRES:

NA.22

product name

D−(−)-α-Phenylglycine, 99%

Saggio

99%

Forma fisica

powder or crystals

Attività ottica

[α]20/D −155°, c = 1 in 1 M HCl

Impiego in reazioni chimiche

reaction type: solution phase peptide synthesis

Colore

white

Punto di fusione

302 °C (dec.) (lit.)

applicazioni

detection

Stringa SMILE

N[C@@H](C(O)=O)c1ccccc1

InChI

1S/C8H9NO2/c9-7(8(10)11)6-4-2-1-3-5-6/h1-5,7H,9H2,(H,10,11)/t7-/m1/s1
ZGUNAGUHMKGQNY-SSDOTTSWSA-N

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

302.0 °F - closed cup

Punto d’infiammabilità (°C)

150 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

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Syntheses and highly enantioselective fluorescent recognition of α-aminocarboxylic acid anions using chiral oxacalix[2]arene[2]bisbinaphthes.

Kuoxi Xu et al.

Chirality, 24(8), 646-651 (2012-05-24)

The triazine-based bisbinaphthyl crown ethers oxacalix[2]arene[2]bisbinaphthes R-1, R-2, R-3 and S-1, S-2, S-3 were synthesized. The interactions of these compounds with various α-aminocarboxylic acid anions were studied. The crown ethers were found to carry out highly enantioselective fluorescent recognition of

Conformational study of jet-cooled L-phenylglycine.

Hyung Min Kim et al.

The Journal of chemical physics, 128(18), 184313-184313 (2008-06-06)

We investigated the conformational structures of L-phenylglycine in the gas phase by photoionization and double resonance spectroscopy techniques as well as high-level ab initio calculations. The UV-UV and IR-UV double resonance spectroscopy suggested that there exists only one conformer that

A straightforward three-component synthesis of alpha-amino esters containing a phenylalanine or a phenylglycine scaffold.

Caroline Haurena et al.

The Journal of organic chemistry, 75(8), 2645-2650 (2010-03-23)

A range of alpha-amino esters has been synthesized in good to high yields using a straightforward three-component reaction among preformed or in situ generated aromatic or benzylic organozinc reagents, primary or secondary amines, and ethyl glyoxylate. The procedure, which is

Isolation and characterization of a benzoylformate decarboxylase and a NAD+/NADP+-dependent benzaldehyde dehydrogenase involved in D-phenylglycine metabolism in Pseudomonas stutzeri ST-201.

Choedchai Saehuan et al.

Biochimica et biophysica acta, 1770(11), 1585-1592 (2007-10-06)

Following induction with D-phenylglycine both d-phenylglycine aminotransferase activity and benzoylformate decarboxylase activity were observed in cultures of Pseudomonas stutzeri ST-201. Induction with benzoylformate, on the other hand, induced only benzoylformate decarboxylase activity. Purification of the benzoylformate decarboxylase, followed by N-terminal

Investigation and characterization of liquid two-phase systems for the separation of crystal mixtures by interfacial partitioning.

Martijn A Hoeben et al.

Biotechnology and bioengineering, 93(4), 607-617 (2006-01-06)

The interfacial partitioning behavior of ampicillin and phenylglycine crystals in different two-phase systems has been investigated. The two-phase systems employed are water/dodecane, water/1-butanol, and water/pentane/methanol. By means of partition experiments and microscopic imaging, it has been shown that the mechanism

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