91309-68-1

Basic information

• Product Name: 1,2-Dichloro-4-((Z)-2-chloro-vinyl)-benzene
• Synonyms: 1,2-Dichloro-4-((Z)-2-chloro-vinyl)-benzene
• CAS NO: 91309-68-1
• Molecular Weight: 207.487
• Mol File: 91309-68-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,2-Dichloro-4-((Z)-2-chloro-vinyl)-benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Dichloro-4-((Z)-2-chloro-vinyl)-benzene(91309-68-1)
• EPA Substance Registry System: 1,2-Dichloro-4-((Z)-2-chloro-vinyl)-benzene(91309-68-1)

Safety Data

• Hazardous Substances Data: 91309-68-1(Hazardous Substances Data)

Upstream product

• 91309-67-0 3-Chloro-3-(3,4-dichloro-benzyl)-3H-diazirine 
• 2039-83-0 3,4-dichlorostyrene 
• 691-38-3 (Z)-4-methyl-2-pentene 

Relevant articles and documents

INVESTIGATIONS ON REACTIONS OF CHLORINE DIOXIDE AND SODIUM CHLORITE WITH ORGANIC COMPOUNDS. PART XXXV. REACTIONS OF CHLORINE DIOXIDE WITH RING-SUBSTITUTED STYRENES

Reactions of chlorine dioxide with ring substituted styrenes (1a-n) in carbon tetrachloride at 52-54 deg C were studied.The reaction products were isolated and characterised.It has been found that methyl-, chloro-, nitrostyrenes and 4-methoxystyrene are attacked by chlorine dioxide exclusively on the vinyl group, to yield the corresponding α-chloroacetophenones (2), diastereoisomers of β-chlorostyrene (6,7), oxidation products (8,9) and some polymers.Oxidation of its phenolic hydroxyl groups and vinyl polymerization took place in hydroxystyrenes.

Photolysis of 3-Chlorodiazirine in the Presence of Alkenes: Orientational Factors in the Intermolecular Interception of Chlorocarbene by Alkenes

The stereochemistry of the 1,2-H shift of photolytically generated benzylchlorocarbene is significantly affected by aryl substituents and by the addition of an alkene.