1600528-32-2

Basic information

• Product Name: (E)-1-(2,3-dichloroprop-1-en-1-yl)-4-methylbenzene
• Synonyms: (E)-1-(2,3-dichloroprop-1-en-1-yl)-4-methylbenzene
• CAS NO: 1600528-32-2
• Molecular Weight: 201.095
• Mol File: 1600528-32-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (E)-1-(2,3-dichloroprop-1-en-1-yl)-4-methylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-(2,3-dichloroprop-1-en-1-yl)-4-methylbenzene(1600528-32-2)
• EPA Substance Registry System: (E)-1-(2,3-dichloroprop-1-en-1-yl)-4-methylbenzene(1600528-32-2)

Safety Data

• Hazardous Substances Data: 1600528-32-2(Hazardous Substances Data)

Upstream product

• 2749-96-4 4-methylphenylallene 
• 104-87-0 4-methyl-benzaldehyde 
• 622-97-9 1-ethenyl-4-methylbenzene 
• 17343-75-8 1-(2,2-dibromocyclopropyl)-4-methylbenzene 

Relevant articles and documents

Chlorination of phenylallene derivatives with 1-chloro-1,2-benziodoxol-3-one: Synthesis of vicinal-dichlorides and chlorodienes

Allyl and vinyl chlorides represent important structural motifs in organic chemistry. Herein is described the chemoselective and regioselective reaction of aryl- and α-substituted phenylallenes with the hypervalent iodine (HVI) reagent 1-chloro-1,2-benz-iodoxol-3-one. The reaction typically results in vicinal dichlorides, except with proton-containing α-alkyl substituents, which instead give chlorinated dienes as the major product. Experimental evidence suggests that a radical mechanism is involved.