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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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Shohei Tashiro et al.
Inorganic chemistry, 50(1), 4-6 (2010-12-01)
The optically active cobalt(III) complex with chiral cyclen, (2S,5S,8S,11S)-2,5,8,11-tetraethyl-1,4,7,10-tetraazacyclododecane, preferentially binds to D-phenylglycine (D-Phg) or D-t-leucine (D-t-Leu) rather than L-Phg or L-t-Leu, respectively, with 20% de in dimethyl sulfoxide at 293 K. Comparative studies on the crystal structures of cobalt(III)
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
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
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
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
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