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P25485

Sigma-Aldrich

D−(−)-α-Phenylglycin

99%, detection

Synonym(e):

(R)-(−)-2-Phenylglycin, D-2-Phenylglycin, R-(−)-α-Aminophenylessigsäure

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About This Item

Lineare Formel:
C6H5CH(NH2)CO2H
CAS-Nummer:
875-74-1
Molekulargewicht:
151.16
Beilstein:
2208676
EG-Nummer:
212-876-3
MDL-Nummer:
MFCD00008061
UNSPSC-Code:
12352209
PubChem Substanz-ID:
24898336
NACRES:
NA.22

product name

D−(−)-α-Phenylglycin, 99%

Assay

99%

Form

powder or crystals

Optische Aktivität

[α]20/D −155°, c = 1 in 1 M HCl

Eignung der Reaktion

reaction type: solution phase peptide synthesis

Farbe

white

mp (Schmelzpunkt)

302 °C (dec.) (lit.)

Anwendung(en)

detection

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-/m1/s1

InChIKey

ZGUNAGUHMKGQNY-SSDOTTSWSA-N

Verwandte Kategorien

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

302.0 °F - closed cup

Flammpunkt (°C)

150 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

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Jian-Lian Chen et al.
Analytica chimica acta, 718, 130-137 (2012-02-07)
Three different approaches for immobilizing cross-linked chitosan molecules (CS-s) in sol-gel phases to form chiral OT-CEC capillaries were comparatively investigated in this study. To synthesize column I, a bare capillary was first silanized with triethoxysilane (TEOS) and then reacted with
Motohiro Akazome et al.
The Journal of organic chemistry, 75(3), 660-665 (2010-01-07)
In terms of chiral recognition for racemic aryl methyl sulfoxides in the solid state, three kinds of crystalline (S)-alkylglycyl-(S)-phenylglycines were examined as potential dipeptides host molecules. When (S)-alanyl-(S)-phenylglycines [(S,S)-Ala-Phg] crystallized with aryl methyl sulfoxides, the stereochemistry of preferentially included sulfoxides
Aaron D Mills et al.
Bioorganic & medicinal chemistry letters, 20(1), 87-91 (2009-12-04)
A developing therapy of cystic fibrosis caused by the DeltaF508 mutation in CFTR employs correction of defective CFTR chloride channel gating by a 'potentiator' and of defective CFTR protein folding by a 'corrector'. Based on SAR data for phenylglycine-type potentiators
Hyung Min Kim et al.
The Journal of chemical physics, 128(4), 041104-041104 (2008-02-06)
Photo-oxidation of amino acids is known to generate reactive protein radicals that lead to lethal disorders. We investigated photoionization of hydrated phenylglycine complexes in the gas phase and found that the excess internal energy from photoionization drives decarboxylation in competition
Yvonne J Mast et al.
Journal of biotechnology, 155(1), 63-67 (2010-12-15)
Pristinamycin I (PI), a streptogramin type B antibiotic produced by Streptomyces pristinaespiralis, contains the aproteinogenic amino acid L-phenylglycine. Recent sequence analysis led to the identification of a set of putative phenylglycine biosynthetic genes. Successive inactivation of the individual genes resulted
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