L-Phenylalanin amide hydrochloride

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Names

[ CAS No. ]:
65864-22-4

[ Name ]:
L-Phenylalanin amide hydrochloride

[Synonym ]:
(2S)-2-amino-3-phenylpropanamide,hydrochloride
Phenylalaninamide hydrochloride (1:1)
Benzenepropanamide, α-amino-, (αS)-, hydrochloride (1:1)
MFCD00039083
H-Phe-NH2.HCl
L-Phenylalanin amide hydrochloride

Chemical & Physical Properties

[ Boiling Point ]:
356.9ºC at 760 mmHg

[ Melting Point ]:
234ºC

[ Molecular Formula ]:
C9H13ClN2O

[ Molecular Weight ]:
200.665

[ Flash Point ]:
169.7ºC

[ Exact Mass ]:
200.071640

[ PSA ]:
69.11000

[ LogP ]:
2.24430

[ Index of Refraction ]:
19 ° (C=2, H2O)

[ Storage condition ]:
Store at RT.

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

Precursor & DownStream

Precursor

  • Methyl L-phenylalaninate hydrochloride
  • L-Phenylalanine
  • Boc-L-phenylalanine
  • H-DL-Phe-NH2.HCl
  • DL-Phenylalanine
  • dl-phenylalanine methyl ester hydrochloride
  • H-Phe-NH2

DownStream

  • H-Phe-NH2
  • Endomorphin-2
  • N-Carbobenzyloxy-L-alanine
  • benzyl N-[2-benzylsulfanyl-1-[(1-carbamoyl-2-phenyl-ethyl)carbamoyl]ethyl]carbamate
  • (2S)-N-[(2S)-1-amino-1-oxo-3-phenylpropan-2-yl]pyrrolidine-2-carboxamide
  • N-T-BOC-MET-ASP-PHE AMIDE
  • H-Asp-Phe-NH2

Articles

Modified amino acids and peptides as substrates for the intestinal peptide transporter PepT1.

Eur. J. Biochem. 267(12) , 3723-8, (2000)

The binding affinities of a number of amino-acid and peptide derivatives by the mammalian intestinal peptide transporter PepT1 were investigated, using the Xenopus laevis expression system. A series o...

Enantioseparation of dansyl amino acids by ligand-exchange capillary electrophoresis with zinc(II)-L-phenylalaninamide complex.

J. Sep. Sci. 32 , 3209-3214, (2009)

A novel method of chiral ligand-exchange CE was developed with L-amino acylamides as a chiral ligand and zinc(II) as a central ion. It has been demonstrated that these chiral complexes, such as Zn(II)...

In vitro selection of DNA aptamers that bind L-tyrosinamide.

Bioorg. Med. Chem. 9(10) , 2543-8, (2001)

We have applied SELEX (Systematic Evolution of Ligands by EXponential enrichment), a combinatorial method that employs biopolymers for drug discovery, to identify single stranded DNA sequences able to...


More Articles


Related Compounds

  • H-Pro-Phe-NH2 · HCl
  • Z-PRO-PHE-NH2
  • (2S)-N-[(2S)-1-amino-1-oxo-3-phenylpropan-2-yl]pyrrolidine-2-carboxamide
  • L-Val-L-Leu-amide hydrochloride
  • l-tyrosinamide hydrochloride
  • L-4-nitrophenylalanyl-L-prolinamide hydrochloride
  • N-cyclopropyl-2-oxooxazolidine-3-sulfonamide
  • 3-Nitro-2-[4-(3-pyridin-2-ylprop-2-ynylidene)piperidin-1-yl]pyridine
  • 2-(4-(3-(3,5-Difluoro-4-methoxyphenyl)prop-2-yn-1-ylidene)piperidin-1-yl)-3-nitropyridine
  • 3-(2-Methoxy-ethoxy)-7H-[1,7]naphthyridin-8-one
  • 2-(Propan-2-yloxy)-6-(pyrrolidin-3-yl)pyridine
  • 2-(2,2,2-Trifluoro-1-methoxyethyl)aniline
  • Methyl 2-[1-[2-[2-(2-oxo-1-piperidinyl)phenyl]ethyl]-3-pyrrolidinyl]benzoate
  • (6-Imidazol-1-ylpyrimidin-4-yl)hydrazine
  • 2-Methyl-1-phenyl-3-(2-phenylphenyl)benzene
  • 5-bromo-N-[(dimethylamino)methylene]-3-methyl-2-Pyridinecarboxamide
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