1016669-67-2

Basic information

• Product Name: ((1R,2R)-2-Methoxycarbonylamino-cyclohexyl)-carbamic acid methyl ester
• Synonyms: ((1R,2R)-2-Methoxycarbonylamino-cyclohexyl)-carbamic acid methyl ester
• CAS NO: 1016669-67-2
• Molecular Weight: 230.264
• Mol File: 1016669-67-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: ((1R,2R)-2-Methoxycarbonylamino-cyclohexyl)-carbamic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: ((1R,2R)-2-Methoxycarbonylamino-cyclohexyl)-carbamic acid methyl ester(1016669-67-2)
• EPA Substance Registry System: ((1R,2R)-2-Methoxycarbonylamino-cyclohexyl)-carbamic acid methyl ester(1016669-67-2)

Safety Data

• Hazardous Substances Data: 1016669-67-2(Hazardous Substances Data)

Upstream product

• 79-22-1 methyl chloroformate 
• 32044-22-7 (1R,2R)-1,2-diaminocyclohexane tartrate 
• 20439-47-8 (1R,2R)-1,2-diaminocyclohexane 

Downstream Products

• 68737-65-5 (R,R)-N,N'-dimethyl-1,2-diaminocyclohexane 

Relevant articles and documents

A new sparteine surrogate for asymmetric deprotonation of N-Boc pyrrolidine

(Chemical Equation Presented) The s-BuLi complex of a cyclohexane-derived diamine is as efficient as s-BuLi/(-)-sparteine for the asymmetric deprotonation of N-Boc pyrrolidine. This is the first example of high enantioselectivity using a non-sparteine-like diamine in such reactions. The ( S, S)-diamine is a useful (+)-sparteine surrogate and was utilized in short syntheses of (-)-indolizidine 167B and an intermediate for the synthesis of the CCK antagonist (+)-RP 66803.