103659-57-0

Basic information

• Product Name: 1-chloro-2-methyl-4-phenylbut-1-ene
• Synonyms: 1-chloro-2-methyl-4-phenylbut-1-ene
• CAS NO: 103659-57-0
• Molecular Weight: 180.677
• Mol File: 103659-57-0.mol

Chemical Properties

• CAS DataBase Reference: 1-chloro-2-methyl-4-phenylbut-1-ene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-chloro-2-methyl-4-phenylbut-1-ene(103659-57-0)
• EPA Substance Registry System: 1-chloro-2-methyl-4-phenylbut-1-ene(103659-57-0)

Safety Data

• Hazardous Substances Data: 103659-57-0(Hazardous Substances Data)

Upstream product

• 930-68-7 cyclohexenone 
• 103659-56-9 1,1-dichloro-2-methyl-4-phenylbut-1-ene 
• 103659-47-8 1,1,1-trichloro-2-hydroxy-2-methyl-4-phenylbutane 

Relevant articles and documents

Titanocene(II)-promoted carbonyl alienation utilizing 1, 1-dichloroalk-1-enes

Treatment of 1,1-dichloroalk-1-enes with Cp2Ti[P(OEt) 3]2 produced organotitanium species, which afford allenes on treatment with aldehydes and ketones The Royal Society of Chemistry 2005.

Chromium(II) Reduction of Trichloromethyl Carbinols and their Corresponding Ethers: One-step Synthesis of Z-Vinyl Chlorides

Secondary trichloromethyl carbinols and their corresponding ethers can be reduced by chemically or electrochemically generated chromium(II) chloride to form Z-monochlorovinyl compounds in one step.In the presence of a carboxy function in the α-position an E-double bond is formed.Tertiary cabinols favour the formation of dichlorovinyl compounds and rearranged carbonyl compounds.Product ratios can be altered drastically by a change in the reaction conditions; this sheds light on the reaction mechanism.