Ac-Phe-OH

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Names

[ CAS No. ]:
2018-61-3

[ Name ]:
Ac-Phe-OH

[Synonym ]:
D-Phenylalanine, N-acetyl-
N-Acetyl-3-phenyl-L-alanine
(2R)-2-acetamido-3-phenylpropanoic acid
N-Acetyl-D-phenylalanine
N-Acetyl-l-Phenylalanine
Acetyl-L-phenylalanine
(S)-2-Acetamido-3-phenylpropanoic acid
EINECS 217-959-8
N-acetyl-D,L-phenylalanine
(2S)-2-acetamido-3-phenylpropanoic acid
L-N-Acetylphenylalanine
MFCD00063158
Ac-Phe-OH
Acetyl-D-Phenylalanine
acetylphenylalanine
Ac-D-Phe-OH

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
453.9±38.0 °C at 760 mmHg

[ Melting Point ]:
171-173 °C(lit.)

[ Molecular Formula ]:
C11H13NO3

[ Molecular Weight ]:
207.226

[ Flash Point ]:
228.3±26.8 °C

[ Exact Mass ]:
207.089539

[ PSA ]:
66.40000

[ LogP ]:
0.78

[ Vapour Pressure ]:
0.0±1.2 mmHg at 25°C

[ Index of Refraction ]:
1.548

MSDS

Safety Information

[ Hazard Codes ]:
Xi

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2924299090

Synthetic Route

Precursor & DownStream

Precursor

  • L-Phenylalanine
  • Ethanoic anhydride
  • acetic acid
  • methyl 2-acetamido-3-phenyl-prop-2-enoate
  • 2-Acetamidoacrylic acid
  • Methyl acetyl-D-phenylalaninate

DownStream

  • (R)-(-)-1-[(4-chlorophenyl)phenylmethyl]piperazine N-acetyl-L-phenylalanine salt
  • 1-[(S)-(4-Chlorophenyl)(phenyl)methyl]piperazine
  • Boc-Cha-OH
  • L-Phenylalanine,N-acetyl-, hydrazide
  • Methyl N-acetyl-L-phenylalaninate
  • N-Acetyl-DL-phenylalanine
  • Ac-Phe-Phe-OH
  • ethyl 2-[(2-acetamido-3-phenyl-propanoyl)amino]-3-[4-[bis(2-chloroethyl)amino]phenyl]propanoate
  • L-Phenylalanine,N-acetyl-, 4-nitrophenyl ester
  • 2-acetamido-3-(4-nitrophenyl)propanoic acid

Customs

[ HS Code ]: 2924299090

[ Summary ]:
2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Peptide synthesis catalyzed by an antibody containing a binding site for variable amino acids.

Science 265 , 234, (1994)

Monoclonal antibodies, induced with a phosphonate diester hapten, catalyzed the coupling of p-nitrophenyl esters of N-acetyl valine, leucine, and phenylalanine with tryptophan amide to form the corres...

Studies on the mechanism for renal elimination of N-acetylphenylalanine: its pathophysiologic significance in phenylketonuria.

J. Lab. Clin. Med. 105(1) , 132-8, (1985)

To elucidate the mechanism and biologic significance of urinary occurrence of N-acetylphenylalanine in phenylketonuria, the metabolic fate of N-acetylphenylalanine was studied in rats. In vivo and in ...

Molecular dynamics (MD) simulations for the prediction of chiral discrimination of N-acetylphenylalanine enantiomers by cyclomaltoheptaose (beta-cyclodextrin, beta-CD) based on the MM-PBSA (molecular mechanics-Poisson-Boltzmann surface area) approach.

Carbohydr. Res. 339(11) , 1961-6, (2004)

Molecular dynamics (MD) simulations were performed for the prediction of chiral discrimination of N-acetylphenylalanine enantiomers by cyclomaltoheptaose (beta-cyclodextrin, beta-CD). Binding free ene...


More Articles


Related Compounds

  • Ac-Phe-Phe-OH
  • Ac-Phe-Lys-OH
  • Ac-Phe-Tyr-OH
  • Ac-Phe-Trp-OH
  • Ac-Phe-3,5-diiodo-Tyr-OH
  • Ac-Phe-Orn-Pro-D-Cha-Trp-Arg-OH