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Key Documents

Altri documenti

237647

Sigma-Aldrich

L−(+)-α-Phenylglycine

99%

Sinonimo/i:

(S)-(+)-2-Phenylglycine, S-(+)-α-Aminophenylacetic acid, L-2-Phenylglycine

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About This Item

Formula condensata:
C6H5CH(NH2)CO2H
Numero CAS:
2935-35-5
Peso molecolare:
151.16
Beilstein:
2208675
Numero CE:
220-909-8
Numero MDL:
MFCD00064403
Codice UNSPSC:
12352209
ID PubChem:
24854260
NACRES:
NA.22

Saggio

99%

Forma fisica

powder

Attività ottica

[α]20/D +155°, c = 1 in 1 M HCl

Impiego in reazioni chimiche

reaction type: solution phase peptide synthesis

Punto di fusione

>300 °C (lit.)

applicazioni

peptide synthesis

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-/m0/s1
ZGUNAGUHMKGQNY-ZETCQYMHSA-N

Applicazioni

Chiral starting material.

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)

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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L-β-Homoserine ≥98.0% (TLC)

Sigma-Aldrich

03694

L-β-Homoserine

DL-2-Phenylglycinol AldrichCPR

Sigma-Aldrich

CDS003505

DL-2-Phenylglycinol

Henry Kurniawan et al.
Cell metabolism, 31(5), 920-936 (2020-03-28)
Regulatory T cells (Tregs) maintain immune homeostasis and prevent autoimmunity. Serine stimulates glutathione (GSH) synthesis and feeds into the one-carbon metabolic network (1CMet) essential for effector T cell (Teff) responses. However, serine's functions, linkage to GSH, and role in stress responses in
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
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