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Merck
CN

P25507

2-Phenylglycine

95%

Synonym(s):

DL-α-Phenylglycine, (±)-α-Aminophenylacetic acid

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About This Item

Linear Formula:
C6H5CH(NH2)COOH
CAS Number:
2835-06-5
Molecular Weight:
151.16
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
24898337
EC Number:
220-608-1
Beilstein/REAXYS Number:
3197862
MDL number:
MFCD00064402

Key Documents

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Product Name

2-Phenylglycine, 95%

InChI

1S/C8H9NO2/c9-7(8(10)11)6-4-2-1-3-5-6/h1-5,7H,9H2,(H,10,11)

InChI key

ZGUNAGUHMKGQNY-UHFFFAOYSA-N

SMILES string

NC(C(O)=O)c1ccccc1

assay

95%

form

powder or crystals

reaction suitability

reaction type: solution phase peptide synthesis

color

white to faint yellow

mp

290 °C (subl.) (lit.)

application(s)

detection

Quality Level

200

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Related Categories

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
WXBF7842V
WXBF5166V
BCCG2259
BCCB0775
BCBS9536V

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Kuoxi Xu et al.
Chirality, 24(8), 646-651 (2012-05-24)
The triazine-based bisbinaphthyl crown ethers oxacalix[2]arene[2]bisbinaphthes R-1, R-2, R-3 and S-1, S-2, S-3 were synthesized. The interactions of these compounds with various α-aminocarboxylic acid anions were studied. The crown ethers were found to carry out highly enantioselective fluorescent recognition of
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
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
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)
Ulrike Müller et al.
Metabolic engineering, 8(3), 196-208 (2006-02-10)
D-phenylglycine (D-Phg) is an important side chain building block for semi-synthetic penicillins and cephalosporins such as ampicillin and cephalexin. To produce d-Phg ultimately from glucose, metabolic engineering was applied. Starting from phenylpyruvate, which is the direct precursor of L-phenylalanine, an
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