41013-43-8

Basic information

• Product Name: 2(R),3(S)-diaminocyclohexane
• CAS NO: 41013-43-8
• Molecular Weight: 114.191
• Mol File: 41013-43-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2(R),3(S)-diaminocyclohexane(CAS DataBase Reference)
• NIST Chemistry Reference: 2(R),3(S)-diaminocyclohexane(41013-43-8)
• EPA Substance Registry System: 2(R),3(S)-diaminocyclohexane(41013-43-8)

Safety Data

• Hazardous Substances Data: 41013-43-8(Hazardous Substances Data)

Upstream product

• 2802-07-5 1,3-cyclohexanedionedioxime 
• 108-45-2 m-phenylenediamine 
• 931-16-8 (+/-)-trans-2-aminocyclohexanol 
• 110-83-8 cyclohexene 
• 286-20-4 cyclohexane-1,2-epoxide 
• 286-18-0 7-azabicyclo<4.1.0>heptane 
• 2562-37-0 1-nitrocyclohexene 
• 71172-32-2 trans-1,2-dinitrocyclohexane 
• 492-99-9 1,2-cyclohexanedionedioxime 
• 286-18-0 7-azabicyclo[4.1.0]heptane 

Downstream Products

• 13291-61-7 trans-1,2-Cyclohexanediaminetetraacetic acid 
• 3187-83-5 rac-trans-N,N'-bis(salicylidene)-1,2-cyclohexanediamine 
• 176776-60-6 2,2′-[(±)-1,2-cyclohexanediylbis[(E)-nitrilomethylidyne]]bisphenol 

Relevant articles and documents

The stereospecific addition of hydroxylamines to α,β-unsaturated sulfones, nitriles and nitro compounds

N-Alkyl hydroxylamines have been shown to undergo a highly stereospecific cis addition to α,β-unsaturated sulfones, nitriles and nitro compounds.

A diamine-exchange reaction of dihydropyrazines

Dihydropyrazines reacted with 1,2-diamines to form tetraazadecalins as intermediates, and then the reaction proceeded forward to dissociate into alternate dihydropyrazine and diamine, or backward to dissociate into the starting materials in certain equilibrium. The product distribution is controlled by diamine-exchange equilibrium reaction. The various equilibrium reactions were analyzed by NMR spectroscopy.