(S)-Benzyl 1-(1H-benzo[d][1,2,3]triazol-1-yl)-1-oxo-3-phenylpropan-2-ylcarbamate

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Names

[ CAS No. ]:
769922-77-2

[ Name ]:
(S)-Benzyl 1-(1H-benzo[d][1,2,3]triazol-1-yl)-1-oxo-3-phenylpropan-2-ylcarbamate

Chemical & Physical Properties

[ Molecular Formula ]:
C23H20N4O3

[ Molecular Weight ]:
400.43000

[ Exact Mass ]:
400.15400

[ PSA ]:
86.11000

[ LogP ]:
4.00010

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ RIDADR ]:
NONH for all modes of transport

Precursor & DownStream

Precursor

DownStream

  • H-Gly-Phe-Ser-OH
  • (S)-Cbz-Phenylalaninol
  • Z-Phe-Met-OH
  • Z-Phe-Val-OH
  • Z-Phe-Phe-OH
  • Z-Phe-Pro-OH
  • Z-Phe-Gly-Gly-OH

Articles

Benzotriazole-mediated syntheses of depsipeptides and oligoesters.

J. Org. Chem. 76 , 4884-4893, (2011)

Reactions of O-Pg(α-hydroxyacyl)benzotriazoles with (a) unprotected α-hydroxycarboxylic acids, (b) amino acids, and (c) amines afforded, respectively, chirally pure (a) oligoesters, (b) depsidipeptide...

Efficient preparation of aminoxyacyl amides, aminoxy hybrid peptides, and alpha-aminoxy peptides.

J. Org. Chem. 74th ed.,, 8690-8694, (2009)

N-(Pg-alpha-aminoxy acids) 1a-g are converted to N-(Pg-alpha-aminoxyacyl)benzotriazoles 2a-g, which react under mild conditions with amines, alpha-amino acids/alpha-dipeptides, and alpha-aminoxy acids...

Abdelmajeid, A.; Tala, S. R.; Amine, M. S.; Katritzky, A. R.

Synthesis , 2995-3005, (2011)


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