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Merck
CN

P2376

L-Phenylalaninamide hydrochloride

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About This Item

Empirical Formula (Hill Notation):
C9H12N2O · HCl
CAS Number:
Molecular Weight:
200.67
PubChem Substance ID:
UNSPSC Code:
12352200
Beilstein/REAXYS Number:
3915662
MDL number:
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SMILES string

Cl.N[C@@H](Cc1ccccc1)C(N)=O

InChI

1S/C9H12N2O.ClH/c10-8(9(11)12)6-7-4-2-1-3-5-7;/h1-5,8H,6,10H2,(H2,11,12);1H/t8-;/m0./s1

InChI key

KLHLGTPNBQXSJT-QRPNPIFTSA-N

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Biochem/physiol Actions

L-Phenylalaninamide hydrochloride is an amino acid amide.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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A V Chetkauskaĭte et al.
Zhurnal evoliutsionnoi biokhimii i fiziologii, 24(4), 465-470 (1988-07-01)
Synthesis of peptides during polymerization of GlyNH2 and PheNH2 has been demonstrated by means of gel-chromatography and thin-layer chromatography. The optima of pH and temperature have been estimated for the reaction. Grem's salt, tripolyphosphate and pyrophosphate were shown to cause
Seiji Okazaki et al.
Acta crystallographica. Section D, Biological crystallography, 64(Pt 3), 331-334 (2008-03-08)
The crystal structures of D-amino-acid amidase (DAA) from Ochrobactrum anthropi SV3 in complex with L-phenylalanine and with L-phenylalanine amide were determined at 2.3 and 2.2 A resolution, respectively. Comparison of the L-phenylalanine amide complex with the D-phenylalanine complex reveals that
Ravi Bhushan et al.
Biomedical chromatography : BMC, 23(12), 1291-1299 (2009-06-03)
Twelve chiral derivatizing reagents (CDRs) were synthesized by substituting one of the fluorine atoms in 1,5-difluoro-2,4-dinitrobenzene (DFDNB) with three optically pure amines [(R)-(-)-1-cyclohexylethylamine, (+)-dehydroabietylamine and (S)-(-)-alpha,4-dimethylbenzylamine], six amino acid amides [L-Ala-NH(2), L-Phe-NH(2), L-Val-NH(2), L-Leu-NH(2), L-Met-NH(2) and D-Phg-NH(2)] and three amino
C Carles et al.
FEBS letters, 212(1), 163-167 (1987-02-09)
This paper is the first to report specific labelling of a native protein at its C-terminal end by carboxypeptidase Y-catalyzed transpeptidation between beta-casein and tritiated Phe amide. A tryptic digest of the radiolabelled protein was resolved by reversed-phase HPLC and
A routine method for alkaline phosphatase assay in pregnancy serum.
D R Pledger et al.
Clinica chimica acta; international journal of clinical chemistry, 122(1), 71-74 (1982-06-16)

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