931-12-4

Basic information

• Product Name: (+/-)-cis-2-chlorocyclohexan-1-amine
• CAS NO: 931-12-4
• Molecular Weight: 133.621
• Mol File: 931-12-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (+/-)-cis-2-chlorocyclohexan-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: (+/-)-cis-2-chlorocyclohexan-1-amine(931-12-4)
• EPA Substance Registry System: (+/-)-cis-2-chlorocyclohexan-1-amine(931-12-4)

Safety Data

• Hazardous Substances Data: 931-12-4(Hazardous Substances Data)

Upstream product

• 110-83-8 cyclohexene 
• 822-87-7 2-Chlorocyclohexanone 
• 1437-81-6 (+/-)-sulfuric acid mono-(trans-2-amino-cyclohexyl ester) 
• 931-16-8 (+/-)-trans-2-aminocyclohexanol 
• 18513-91-2 ((1R,2R)-2-Chloro-cyclohexyl)-phosphoramidic acid diethyl ester 
• 74-90-8 hydrogen cyanide 
• 286-18-0 7-azabicyclo[4.1.0]heptane 
• 1377325-95-5 C₁₆H₂₄ClNO₂S 
• 931-12-4 (+/-)-cis-2-chlorocyclohexan-1-amine 

Downstream Products

• 100385-40-8 optically inactive bis-(trans-2-amino-cyclohexyl)-disulfide 
• 931-12-4 (1S)-cis-2-chloro-1-amino-cyclohexane 
• 872-53-7 cyclopentanealdehyde 
• 117864-55-8 N-[2-(7-aza-norcaran-7-yl)-cyclohexyl]-benzamide 
• 1180536-79-1 (1R,2R)-N-(2-chlorocyclohexyl)benzamide 
• 13908-80-0 1,3-Bis(trans-2-chlorocyclohexyl)urea 
• 108-94-1 cyclohexanone 
• 4098-70-8 cis-ethyl N-2-chlorocyclohexylcarbamate 
• 4098-70-8 trans-ethyl N-2-chlorocyclohexylcarbamate 
• 89796-69-0 cis-(2-Chlor-cyclohexylamino)-methansulfonsaeure 

Relevant articles and documents

Strong hyperconjugative interactions limit solvent and substituent influence on conformational equilibrium: The case of cis-2-halocyclohexylamines

The presence of strong stereoelectronic interactions involving the substituents in cis-2-substituted cyclohexanes may lead to results different from those expected. In this work, we studied the conformational behavior of cis-2-fluoro- (F), cis-2-chloro- (

Catalytic asymmetric ring openings of Meso and terminal aziridines with halides mediated by chiral 1,2,3-triazolium silicates

Catalytic asymmetric chloride and bromide ring openings of meso aziridines with trimethylsilyl halides have been developed using modular chiral 1,2,3-triazolium chlorides as catalysts. Control experiments suggest the reaction pathway involving hypervalent