328123-64-4

Basic information

• Product Name: (S)-(cyclopent-2-en-1-yl)cyclohexane
• Synonyms: (S)-(cyclopent-2-en-1-yl)cyclohexane
• CAS NO: 328123-64-4
• Molecular Weight: 150.264
• Mol File: 328123-64-4.mol

Chemical Properties

• CAS DataBase Reference: (S)-(cyclopent-2-en-1-yl)cyclohexane(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-(cyclopent-2-en-1-yl)cyclohexane(328123-64-4)
• EPA Substance Registry System: (S)-(cyclopent-2-en-1-yl)cyclohexane(328123-64-4)

Safety Data

• Hazardous Substances Data: 328123-64-4(Hazardous Substances Data)

Upstream product

• 941570-75-8 (+)-(S)-hepta-1,6-dien-3-ylcyclohexane 
• 62019-06-1 (E)-2,6-heptadien-1-ol 
• 95514-62-8 (E)-ethyl hepta-2,6-dienoate 
• 821-09-0 n-Pent-4-enyl alcohol 
• 2100-17-6 4-pentenal 
• 41792-05-6 3-chloro-1-heptene 

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

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ω-Ethylenic allylic substrates as alternatives to cyclic substrates in copper- and iridium-catalyzed asymmetric allylic alkylation

"Chemical Equation Presented" A new strategy to access highly enantioenriched cyclic compounds (up to 98%) Is proposed using ω-ethylenic allylic substrates through a one-pot asymmetric allylic alkylation and ring-closing metathesis. Such starting compounds can be seen as synthetic equivalents of cyclic allylic substrates.