1182228-53-0

Basic information

• Product Name: (-)-(R)-3-cyclohexylcyclohex-1-ene
• Synonyms: (-)-(R)-3-cyclohexylcyclohex-1-ene
• CAS NO: 1182228-53-0
• Molecular Weight: 164.291
• Mol File: 1182228-53-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (-)-(R)-3-cyclohexylcyclohex-1-ene(CAS DataBase Reference)
• NIST Chemistry Reference: (-)-(R)-3-cyclohexylcyclohex-1-ene(1182228-53-0)
• EPA Substance Registry System: (-)-(R)-3-cyclohexylcyclohex-1-ene(1182228-53-0)

Safety Data

• Hazardous Substances Data: 1182228-53-0(Hazardous Substances Data)

Upstream product

• 62179-18-4 (2E)-octa-2,7-dien-1-ol 
• 79972-66-0 octa-7-en-2-yn-1-ol 
• 931-51-1 cyclohexylmagnesiumchloride 
• 92747-32-5 (E)-8-chloro-octa-1,6-diene 
• 41309-53-9 C₈H₁₃Cl 
• 1521-51-3 rac-3-bromocyclohexene 
• 931-50-0 cyclohexylmagnesium bromide 

Relevant articles and documents

Construction of enantioenriched cyclic compounds by asymmetric allylic alkylation and ring-closing metathesis

A new approach to highly enantioenriched cyclic compounds (up to 98a€‰% ee) has been developed by using ω-ethylenic allylic substrates in a one-pot asymmetric allylic alkylation and ring-closing metathesis sequence. The starting compounds are synthetic equivalents of cyclic allylic substrates. The method is exemplified with both Cu and Ir catalysts, and chiral phosphoramidite ligands. A new approach to highly enantioenriched cyclic compounds (up to 98a€‰% ee) has been developed by using ω-ethylenic allylic substrates in a one-pot asymmetric allylic alkylation and ring-closing metathesis sequence. The starting compounds are synthetic equivalents of cyclic allylic substrates. The method is exemplified with both Cu and Ir catalysts, and chiral phosphoramidite ligands. Copyright

Dynamic kinetic asymmetric transformation in copper catalyzed allylic alkylation

The first dynamic kinetic asymmetric transformation in copper catalyzed allylic alkylation is reported, with enantioselectivities up to 92%.