358359-38-3

Basic information

• Product Name: Cyclohexanamine, N,5-dimethyl-2-(1-methylethyl)-, (1S,2S,5R)- (9CI)
• Synonyms: Cyclohexanamine, N,5-dimethyl-2-(1-methylethyl)-, (1S,2S,5R)- (9CI)
• CAS NO: 358359-38-3
• Molecular Formula: C₁₁H₂₃N
• Molecular Weight: 169.30702
• Product Categories: ISOPROPYL
• Mol File: 358359-38-3.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Cyclohexanamine, N,5-dimethyl-2-(1-methylethyl)-, (1S,2S,5R)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanamine, N,5-dimethyl-2-(1-methylethyl)-, (1S,2S,5R)- (9CI)(358359-38-3)
• EPA Substance Registry System: Cyclohexanamine, N,5-dimethyl-2-(1-methylethyl)-, (1S,2S,5R)- (9CI)(358359-38-3)

Safety Data

• Hazardous Substances Data: 358359-38-3(Hazardous Substances Data)

Upstream product

• 2216-51-5 (-)-menthol 
• 61548-81-0 (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl methanesulfonate 
• 107535-12-6 (1S,2S,4R)-2-azido-1-isopropyl-4-methylcyclohexane 
• 7231-40-5 (+)-(1R,3S,4S)-neomenthylamine 

Downstream Products

• 52209-29-7 dimethyl-((1R)-neomenthyl)-amine 
• 16508-42-2 trimethyl-((1R)-neomenthyl)-ammonium; iodide 

Relevant articles and documents

Diastereoselective desymmetrization of diarylphosphinous acid-borane amides under Birch reduction

Treatment of diarylphosphinous acid-borane amides possessing chiral amido functionality with an alkali metal solution in liquid ammonia induced a preferential dearomatization of one aryl substituent at phosphorus leading to the formation of non-equimolar amounts of diastereomers. Diastereoselectivity of dearomatization depends strongly on the structure of a chiral auxiliary.