92762-94-2

Basic information

• Product Name: Butanoic acid, 3,4-diamino-4-oxo-, phenylmethyl ester, (3S)-, mono(trifluoroacetate)
• CAS NO: 92762-94-2
• Molecular Formula: C11H14N2O3.C2HF3O2
• Molecular Weight: 336.268
• Mol File: 92762-94-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Butanoic acid, 3,4-diamino-4-oxo-, phenylmethyl ester, (3S)-, mono(trifluoroacetate)(CAS DataBase Reference)
• NIST Chemistry Reference: Butanoic acid, 3,4-diamino-4-oxo-, phenylmethyl ester, (3S)-, mono(trifluoroacetate)(92762-94-2)
• EPA Substance Registry System: Butanoic acid, 3,4-diamino-4-oxo-, phenylmethyl ester, (3S)-, mono(trifluoroacetate)(92762-94-2)

Safety Data

• Hazardous Substances Data: 92762-94-2(Hazardous Substances Data)

Upstream product

• 87421-27-0 N-t-butyloxycarbonyl-L-aspartic acid β-benzyl ester α-amide 
• 76-05-1 trifluoroacetic acid 
• 82825-48-7 α-pentafluorophenyl N-tert-butoxycarbonyl-β-benzyl-L-asparaginate 
• 7536-58-5 BOC-L-aspartic acid 4-benzyl ester 

Downstream Products

• 129280-57-5 N^ε-tert-butoxycarbonylaminocaproyl-β-benzyl-L-asparaginic acid α-amide 
• 94236-47-2 N-tert-butoxycarbonyl-L-leucyl-β-benzyl-L-asparaginic acid α-amide 
• 94236-51-8 Boc-L-Phe-L-Asp(Bzl)-NH₂ 
• 92762-79-3 (tert-butyloxycarbonyl)-L-methionyl-β-benzyl-L-aspartic acid amide 
• 129594-14-5 Z-Orn(Boc)-Asp(OBzl)-NH₂ 
• 94236-49-4 Boc-L-Nle-L-Asp(Bzl)-NH₂ 
• 129280-55-3 N^γ-tert-butoxycarbonylbutyryl-β-benzyl-L-asparaginic acid α-amide 
• 129280-56-4 N^δ-tert-butoxycarbonylaminovaleryl-β-benzyl-L-asparaginic acid α-amide 
• 94236-48-3 Boc-L-Ile-L-Asp(Bzl)-NH₂ 
• 94249-75-9 Boc-L-Pro-L-Asp(Bzl)-NH₂ 

Relevant articles and documents

2-Amino-4-pyrrolidinothieno[2,3-d]pyrimidine-6-carboxylic acid as an N-terminal surrogate in amino acid and peptide analogues

2-Amino-4-pyrrolidinothieno[2,3-d]pyrimidine-6-carboxylic acid (4) (ATPC) is an unnatural amino acid with promise in applications as a building block for the synthesis of peptidomimetics. ATPC was obtained from both 3a and 3b thienopyrimidines by hydrolysis and hydrogenolysis, respectively. The synthesis of eleven ATPC-amino acids and two ATPC-peptides is described. ATPC is incorporated as N-terminal moiety in solution or solid-phase peptide synthesis using Boc or Fmoc methodology and without protection of the ATPC amino group. Georg Thieme Verlag Stuttgart.

SYNTHESIS OF STRUCTURAL ANALOGS OF THE 13-16 FRAGMENT OF GASTRIN, AND THEIR EFFECTS ON GASTRIC SECRETION

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