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Merck
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Documentos

P2376

Sigma-Aldrich

L-Phenylalaninamide hydrochloride

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About This Item

Fórmula empírica (notación de Hill):
C9H12N2O · HCl
Número de CAS:
65864-22-4
Peso molecular:
200.67
Beilstein/REAXYS Number:
3915662
MDL number:
MFCD00039083
UNSPSC Code:
12352200
PubChem Substance ID:
24898314

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_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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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
J F Rehfeld
Clinical chemistry, 44(5), 991-1001 (1998-05-20)
Shortage of reliable plasma assays has hampered studies of cholecystokinin (CCK). The assay problems are low plasma concentrations, extensive molecular heterogeneity, and close homology of CCK to gastrin, which circulates in higher concentrations. To develop an accurate CCK RIA, antibodies
M Mizanur Rahman et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 14(4), 1312-1321 (2007-11-23)
The monomer N'-octadecyl-N(alpha)-(4-vinyl)-benzoyl-L-phenylalanineamide (4) based on L-phenylalanine has been simply but effectively synthesized, and its self-assembling properties have been investigated. FTIR and a variable-temperature (1)H NMR spectroscopic investigation demonstrated that the aggregation of compound 4 in various organic solvents is
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