1055905-29-7

Basic information

• Product Name: ((1R,2S)-2-((E)-1,2-dichloroprop-1-enyloxy)cyclohexyl)benzene
• Synonyms: ((1R,2S)-2-((E)-1,2-dichloroprop-1-enyloxy)cyclohexyl)benzene
• CAS NO: 1055905-29-7
• Molecular Weight: 285.213
• Mol File: 1055905-29-7.mol

Chemical Properties

• CAS DataBase Reference: ((1R,2S)-2-((E)-1,2-dichloroprop-1-enyloxy)cyclohexyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: ((1R,2S)-2-((E)-1,2-dichloroprop-1-enyloxy)cyclohexyl)benzene(1055905-29-7)
• EPA Substance Registry System: ((1R,2S)-2-((E)-1,2-dichloroprop-1-enyloxy)cyclohexyl)benzene(1055905-29-7)

Safety Data

• Hazardous Substances Data: 1055905-29-7(Hazardous Substances Data)

Upstream product

• 1055905-27-5 ((1R,2S)-2-((E)-1,2-dichlorovinyloxy)cyclohexyl)benzene 
• 74-88-4 methyl iodide 
• 34281-92-0 (1S,2R)-trans-2-phenyl-1-cyclohexanol 

Relevant articles and documents

Dichloroenol ethers x-ray analysis in the mechanistic elucidation of ynol ethers formation

X-ray crystallographic data are provided for dichloroenol ethers (S,E)-2-(1-(1,2-dichlorovinyloxy)ethyl)-1,3,5-triisopropylbenzene (2) and (S,E)-2-(1-(1,2-dichloroprop-1-enyloxy)ethyl)-1,3,5-triisopropylbenzene (3). The former forms colorless crystals (or

Ynol ethers from dichloroenol ethers: Mechanistic elucidation through 35Cl labeling

(Chemical Equation Presented) The mechanism of ynol ether formation from dichloroenol ethers, a decades-old transformation, has been studied by experimental and theoretical techniques to determine the relative importance of the Fritsch-Buttenberg-Wichell rearrangement (α-elimination) and β-elimination in the evolution of the intermediate carbenoid.