1012369-67-3

Basic information

• Product Name: (R)-tert-butyl 2-cyclohexyl-5-oxopyrrolidine-1-carboxylate
• Synonyms: (R)-tert-butyl 2-cyclohexyl-5-oxopyrrolidine-1-carboxylate
• CAS NO: 1012369-67-3
• Molecular Weight: 267.368
• Mol File: 1012369-67-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (R)-tert-butyl 2-cyclohexyl-5-oxopyrrolidine-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-tert-butyl 2-cyclohexyl-5-oxopyrrolidine-1-carboxylate(1012369-67-3)
• EPA Substance Registry System: (R)-tert-butyl 2-cyclohexyl-5-oxopyrrolidine-1-carboxylate(1012369-67-3)

Safety Data

• Hazardous Substances Data: 1012369-67-3(Hazardous Substances Data)

Upstream product

• 1012369-57-1 (R)-1-tert-butyl 3-allyl 5-cyclohexyl-2-oxopyrrolidine-1,3-dicarboxylate 
• 109183-71-3 N-(tert-butoxycarbonyl)-L-cyclohexylglycine 
• 1318249-52-3 C₁₉H₃₁NO₆ 
• 1318249-50-1 C₁₉H₂₉NO₇ 

Downstream Products

• 1318249-54-5 BF₄^(1-)*C₁₇H₁₇F₅N₃⁽¹⁺⁾ 
• 872358-02-6 (R)-5-cyclohexylpyrrolidin-2-one 

Relevant articles and documents

N-heterocyclic carbene and Bronsted acid cooperative catalysis: Asymmetric synthesis of trans -γ-Lactams

An efficient enantioselective approach to form trans-γ-lactams in up to 99% yield, 93% ee, and >20/1 dr using unactivated imines has been developed. The cyclohexyl-substituted azolium and the weak base sodium o-chlorobenzoate are most suitable for this tr