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P25507

Sigma-Aldrich

2-Phenylglycine

95%

Sinonimo/i:

DL-α-Phenylglycine, (±)-α-Aminophenylacetic acid

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About This Item

Formula condensata:
C6H5CH(NH2)COOH
Numero CAS:
2835-06-5
Peso molecolare:
151.16
Beilstein:
3197862
Numero CE:
220-608-1
Numero MDL:
MFCD00064402
Codice UNSPSC:
12352209
ID PubChem:
24898337
NACRES:
NA.22

Livello qualitativo

200

Saggio

95%

Stato

powder or crystals

Impiego in reazioni chimiche

reaction type: solution phase peptide synthesis

Colore

white to faint yellow

Punto di fusione

290 °C (subl.) (lit.)

applicazioni

detection

Stringa SMILE

NC(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)
ZGUNAGUHMKGQNY-UHFFFAOYSA-N

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Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
BCCG2259
BCCB0775
BCBS9536V
BCBQ8757V
BCBM4785V

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2,2-Diphenylglycine 98%

Sigma-Aldrich

161918

2,2-Diphenylglycine

Tetra-eptilammonio bromuro ≥99.0% (AT)

Sigma-Aldrich

87301

Tetra-eptilammonio bromuro

Orcinol 97%

Sigma-Aldrich

447420

Orcinol

N-Methylpyrrolidine 97%

Sigma-Aldrich

M79204

N-Methylpyrrolidine

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
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
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
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
James J Lynch et al.
Pain, 125(1-2), 136-142 (2006-06-20)
Gabapentin and pregabalin have been demonstrated, both in animal pain models and clinically, to be effective analgesics particularly for the treatment of neuropathic pain. The precise mechanism of action for these two drugs is unknown, but they are generally believed
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