84553-28-6

Basic information

• Product Name: 1-Chloro-4-((E)-1,2-dichloro-vinyl)-benzene
• Synonyms: 1-Chloro-4-((E)-1,2-dichloro-vinyl)-benzene
• CAS NO: 84553-28-6
• Molecular Weight: 207.487
• Mol File: 84553-28-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-Chloro-4-((E)-1,2-dichloro-vinyl)-benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Chloro-4-((E)-1,2-dichloro-vinyl)-benzene(84553-28-6)
• EPA Substance Registry System: 1-Chloro-4-((E)-1,2-dichloro-vinyl)-benzene(84553-28-6)

Safety Data

• Hazardous Substances Data: 84553-28-6(Hazardous Substances Data)

Upstream product

• 873-73-4 4-n-chlorophenylacetylene 
• 64-19-7 acetic acid 
• 33491-02-0 1-chloro-4-(chloroethynyl)benzene 
• 79-01-6 Trichloroethylene 
• 873-77-8 (4-chlorphenyl)magnesium bromide 

Downstream Products

• 1005500-80-0 N-((4-chlorophenyl)ethynyl)-N,4-dimethylbenzenesulfonamide 

Relevant articles and documents

Transition-Metal-Free One-Step Synthesis of Ynamides

A robust transition-metal-free one-step strategy for the synthesis of ynamides from sulfonamides and (Z)-1,2-dichloroalkenes or alkynyl chlorides is presented. This method is not only effective for internal ynamides but also amenable for terminal ynamides. Various functional groups, even the vinyl moiety, are compatible, and thus, this strategy offers the opportunity for further functionalization.

A Remarkable Steric Effect in Palladium-Catalyzed Grignard Coupling: Regio and Stereoselective Monoalkylation and -arylation of 1,1-Dichloro-1-alkenes

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REACTION DE L'ACIDE PERCHLORIQUE SUR LES PHENYLACETYLENES SUBSTITUES. MISE EN EVIDENCE D'UN MECANISME IONIQUE ET RADICALAIRE

We have studied the reaction of perchloric acid in acetic acid medium on some substituted phenylacetylenes.The ionic and radicalar mechanism is in agreement with the formation of and alkenyl perchlorate which is decomposed according to an homolytic process.