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Merck
CN

344273

(R)-(−)-2-Phenylglycine chloride hydrochloride

97%

Synonym(s):

(R)-α-Aminophenylacetyl chloride hydrochloride, D−(−)−α-Phenylglycine chloride hydrochloride

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About This Item

Linear Formula:
C6H5CH(NH2)COCl·HCl
CAS Number:
39878-87-0
Molecular Weight:
206.07
PubChem Substance ID:
24861238
UNSPSC Code:
12352200
EC Number:
254-668-5
MDL number:
MFCD00039094
Beilstein/REAXYS Number:
5405183

Key Documents

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assay

97%

optical activity

[α]29/D −116°, c = 6 in 1 M HCl

reaction suitability

reaction type: solution phase peptide synthesis

mp

117 °C (dec.) (lit.)

SMILES string

Cl[H].N[C@@H](C(Cl)=O)c1ccccc1

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Resp. Sens. 1 - Skin Corr. 1B - Skin Sens. 1

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

302.0 °F - closed cup

flash_point_c

150 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
08208HE
06121PE
06711KD
05011KD
08703ED

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Kalagouda B Gudasi et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 67(1), 172-177 (2006-09-05)
Phenylglycine hydrazide was synthesized and investigated by X-ray crystallography. It crystallizes in the monoclinic space group P121/c with cell parameters a=5.9459 (18) Angstrom, b=5.1940 (16) Angstrom, c=26.7793 (83) Angstrom and Z=2. Its conformational changes, on complexation with transition metal ions
Li Ming et al.
Journal of mass spectrometry : JMS, 40(8), 1072-1075 (2005-06-18)
A novel mass spectrometric method is applied to rapid, accurate, quantitative analysis of chiral phenylglycine. Transition-metal-bound complex ions containing the chiral phenylglycine are generated by electrospray ionization mass spectrometry and subjected to collision-induced dissociation. The ratio of the two competitive
Kourosh Malek et al.
The journal of physical chemistry. B, 112(5), 1549-1554 (2008-01-18)
Cross-linked enzyme crystals (CLECs) enclose an extensive regular matrix of chiral solvent-filled nanopores, via which ions and solutes travel in and out. Several cross-linked enzyme crystals have recently been used for chiral separation and as biocatalysts. We studied the dynamics
W M Kati et al.
Antimicrobial agents and chemotherapy, 45(9), 2563-2570 (2001-08-15)
In an effort to discover novel, noncarbohydrate inhibitors of influenza virus neuraminidase we hypothesized that compounds which contain positively charged amino groups in an appropriate position to interact with the Asp 152 or Tyr 406 side chains might be bound
S J Conway et al.
Bioorganic & medicinal chemistry letters, 11(6), 777-780 (2001-03-30)
The syntheses of a range of ring and alpha-substituted 4-phosphonophenylglycines are described. A brief discussion of the antagonist activities of compounds 4-10 on group I, II and III metabotropic glutamate (mGlu) receptors expressed in the neonatal rat spinal cord is
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