99266-93-0

Basic information

• Product Name: 3-hydroxy-1-iodo-4-cyclohexyl-1-trans-butene
• CAS NO: 99266-93-0
• Molecular Weight: 280.149
• Mol File: 99266-93-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-hydroxy-1-iodo-4-cyclohexyl-1-trans-butene(CAS DataBase Reference)
• NIST Chemistry Reference: 3-hydroxy-1-iodo-4-cyclohexyl-1-trans-butene(99266-93-0)
• EPA Substance Registry System: 3-hydroxy-1-iodo-4-cyclohexyl-1-trans-butene(99266-93-0)

Safety Data

• Hazardous Substances Data: 99266-93-0(Hazardous Substances Data)

Upstream product

• 23860-35-7 cyclohexylacetic acid chloride 
• 99222-87-4 (E)-4-Chloro-1-cyclohexyl-but-3-en-2-one 
• 99383-46-7 (E)-1-Cyclohexyl-4-iodo-but-3-en-2-one 

Downstream Products

• 99223-04-8 (1R,4R,5S)-4-((E)-(S)-1-Cyclohexylmethyl-3-iodo-allyloxy)-6,6-dimethyl-3-oxa-bicyclo[3.1.0]hexan-2-one 
• 99266-97-4 (1R,4R,5S)-4-((E)-(R)-1-Cyclohexylmethyl-3-iodo-allyloxy)-6,6-dimethyl-3-oxa-bicyclo[3.1.0]hexan-2-one 
• 99223-13-9 (E)-(R)-1-Cyclohexyl-4-iodo-but-3-en-2-ol 

Relevant articles and documents

A HIGHLY EFFICIENT SYNTHESIS OF OPTICALLY PURE γ-IODO ALLYLIC ALCOHOLS AND THEIR CONVERSION INTO VARIOUS OPTICALLY ACTIVE ALLYLIC ALCOHOLS

Kinetic resolution of γ-iodo allylic alcohols 1 by the Sharpless asymmetric epoxidation reaction proceeds with very large rate differences for the two enantiomers, thus providing a highly efficient method for preparation of optically pure 1.The alcohols 1