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237647

Sigma-Aldrich

L−(+)-α-Phenylglycin

99%

Synonym(e):

(S)-(+)-2-Phenylglycin, S-(+)-α-Aminophenylessigsäure, L-2-Phenylglycin

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About This Item

Lineare Formel:
C6H5CH(NH2)CO2H
CAS-Nummer:
2935-35-5
Molekulargewicht:
151.16
Beilstein:
2208675
EG-Nummer:
220-909-8
MDL-Nummer:
MFCD00064403
UNSPSC-Code:
12352209
PubChem Substanz-ID:
24854260
NACRES:
NA.22

Qualitätsniveau

100

Assay

99%

Form

powder

Optische Aktivität

[α]20/D +155°, c = 1 in 1 M HCl

Eignung der Reaktion

reaction type: solution phase peptide synthesis

mp (Schmelzpunkt)

>300 °C (lit.)

Anwendung(en)

peptide synthesis

SMILES String

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

InChIKey

ZGUNAGUHMKGQNY-ZETCQYMHSA-N

Verwandte Kategorien

Anwendung

Chiral starting material.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

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L-β-Homoserin ≥98.0% (TLC)

Sigma-Aldrich

03694

L-β-Homoserin

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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