P25485
D−(−)-α-Phenylglycine
99%, detection
Synonym(s):
(R)-(−)-2-Phenylglycine, D-2-Phenylglycine, R-(−)-α-Aminophenylacetic acid
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About This Item
Linear Formula:
C6H5CH(NH2)CO2H
CAS Number:
Molecular Weight:
151.16
Beilstein:
2208676
EC Number:
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.22
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Product Name
D−(−)-α-Phenylglycine, 99%
Quality Level
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
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
302.0 °F - closed cup
Flash Point(C)
150 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
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