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P25485

D-(-)-α-苯甘氨酸

Name: <SC>D</SC>-(-)-&#945;-苯甘氨酸
Brand: ALDRICH

99%, detection

别名:

(R)-(-)-2-苯基甘氨酸, D-2-苯基甘氨酸, R-(-)-α-氨基苯基乙酸

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关于此项目

线性分子式:

C₆H₅CH(NH₂)CO₂H

化学文摘社编号:

875-74-1

分子量:

151.16

NACRES:

NA.22

PubChem Substance ID:

24898336

UNSPSC Code:

12352209

EC Number:

212-876-3

MDL number:

MFCD00008061

Beilstein/REAXYS Number:

2208676

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属性

产品名称

D-(-)-α-苯甘氨酸, 99%

Quality Level

200

assay

99%

form

powder or crystals

optical activity

[α]20/D −155°, c = 1 in 1 M HCl

reaction suitability

reaction type: solution phase peptide synthesis

color

white

mp

302 °C (dec.) (lit.)

application(s)

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

InChI key

ZGUNAGUHMKGQNY-SSDOTTSWSA-N

说明

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存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

302.0 °F - closed cup

flash_point_c

150 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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(L)-Phenylglycine, but not necessarily other alpha2delta subunit voltage-gated calcium channel ligands, attenuates neuropathic pain in rats.

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

Synthesis of new imidazolidin-2,4-dione and 2-thioxoimidazolidin-4-ones via C-phenylglycine derivatives.

José Alixandre de Sousa Luis et al.

Molecules (Basel, Switzerland), 15(1), 128-137 (2010-01-30)

Hydantoins and their derivatives constitute a group of pharmaceutical compounds with anticonvulsant and antiarrhythmic properties, and are also used against diabetes. N-3 and C-5 substituted imidazolidines are examples of such products. As such, we have developed a synthesis of 2,4-dione

Chiral recognition of α-amino acids by an optically active (2S,5S,8S,11S)-2,5,8,11-tetraethyl cyclen cobalt(III) complex.

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)

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全球贸易项目编号

货号	GTIN
P25485-100G	04061834364023
P25485-25G	04061834364030