1252809-39-4

Basic information

• Product Name: (3S,4S)-1-benzyl-4-(tert-butoxycarbonyl)amino-4-methoxycarbonyl-3-methyl-2-oxoazepane
• Synonyms: (3S,4S)-1-benzyl-4-(tert-butoxycarbonyl)amino-4-methoxycarbonyl-3-methyl-2-oxoazepane
• CAS NO: 1252809-39-4
• Molecular Weight: 390.48
• Mol File: 1252809-39-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (3S,4S)-1-benzyl-4-(tert-butoxycarbonyl)amino-4-methoxycarbonyl-3-methyl-2-oxoazepane(CAS DataBase Reference)
• NIST Chemistry Reference: (3S,4S)-1-benzyl-4-(tert-butoxycarbonyl)amino-4-methoxycarbonyl-3-methyl-2-oxoazepane(1252809-39-4)
• EPA Substance Registry System: (3S,4S)-1-benzyl-4-(tert-butoxycarbonyl)amino-4-methoxycarbonyl-3-methyl-2-oxoazepane(1252809-39-4)

Safety Data

• Hazardous Substances Data: 1252809-39-4(Hazardous Substances Data)

Upstream product

• 1252809-37-2 (3S,4S)-4-tert-butoxycarbonyl-4-(tert-butoxycarbonyl)amino-3-methyl-2-oxoazepane 
• 100-39-0 benzyl bromide 
• 1252809-29-2 (3S,4S)-4-[3'-(benzyloxycarbonyl)amino]propyl-4-methoxycarbonyl-3-methyl-2-oxoazetidine 
• 1252809-30-5 (3S,4S)-4-[3-(benzyloxycarbonyl)amino]propyl-1-tert-butoxycarbonyl-4-methoxycarbonyl-3-methyl-2-oxoaze4-methoxycarbonyl-3-methyl-2-oxoazetidine 
• 24424-99-5 di-tert-butyl dicarbonate 
• 1252809-31-6 (3S,4S)-4-(tert-butoxycarbonyl)amino-4-methoxycarbonyl-3-methyl-2-oxoazepane 
• 5874-75-9 methyl (2S)-2-amino-5-[[(benzyloxy)carbonyl]amino]pentanoate hydrochloride 

Downstream Products

• 1315455-75-4 C₂₄H₃₆N₄O₅ 
• 1315455-76-5 C₂₄H₃₆N₄O₄ 
• 1417722-37-2 (3R,4S)-1-benzyl-4-(tert-butoxycarbonyl)amino-4-methoxycarbonyl-3-methylazepane 

Relevant articles and documents

Divergent, stereoselective access to heterocyclic α,α-quaternary- and β2,3,3-amino acid derivatives from a N-Pmp-protected Orn-derived β-lactam

A suitably protected Orn-derived (3S,4S)-β-lactam was used as common intermediate in the synthesis of conformationally constrained (3S,4S)-2-oxoazepane α,α- and (2S,3S)-2-oxopiperidine-β2,3,3-amino acid derivatives. Compared to alternative proc