1447498-11-4

Basic information

• Product Name: (S)-2-(2-((benzyloxy)carbonyl)hydrazinyl)propanoic acid
• Synonyms: (S)-2-(2-((benzyloxy)carbonyl)hydrazinyl)propanoic acid
• CAS NO: 1447498-11-4
• Molecular Weight: 238.243
• Mol File: 1447498-11-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-2-(2-((benzyloxy)carbonyl)hydrazinyl)propanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-(2-((benzyloxy)carbonyl)hydrazinyl)propanoic acid(1447498-11-4)
• EPA Substance Registry System: (S)-2-(2-((benzyloxy)carbonyl)hydrazinyl)propanoic acid(1447498-11-4)

Safety Data

• Hazardous Substances Data: 1447498-11-4(Hazardous Substances Data)

Upstream product

• 21028-15-9 (S)-α-hydrazinopropionic acid 
• 57710-80-2 1-benzyloxycarbonyl-1Hbenzo[d][1.2.3]triazole 

Downstream Products

• 1447498-15-8 (S)-benzyl 2-(1-((3-(1H-imidazol-1-yl)propyl)amino)-1-oxopropan-2-yl)hydrazinecarboxylate 

Relevant articles and documents

Syntheses of hydrazino peptides and conjugates

(α-Benzyloxycarbonyl-aminoacyl)benzotriazolides (Cbz = benzyloxycarbonyl) underwent a coupling reaction with α-hydrazino acids under microwave irradiation to form hybrid hydrazino dipeptides (42-71 %). Chiral acylations of β-N-Cbz-α-hydrazino acylbenzotriazolides were successfully carried out with N-, S-, O-, and C-nucleophiles in yields of 49-88 %. Benzyloxycarbonyl-protected hybrid hydrazino dipeptides and benzyloxycarbonyl-protected hydrazino aminoacyl conjugates with N-, S-, O-, and C-nucleophiles were prepared by using benzotriazole methodology. Copyright