22013-79-2

Basic information

• Product Name: Benzene, 1-chloro-4-(1,2-dibromo-2-nitroethyl)-
• CAS NO: 22013-79-2
• Molecular Formula: C8H6Br2ClNO2
• Molecular Weight: 343.402
• Mol File: 22013-79-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzene, 1-chloro-4-(1,2-dibromo-2-nitroethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-chloro-4-(1,2-dibromo-2-nitroethyl)-(22013-79-2)
• EPA Substance Registry System: Benzene, 1-chloro-4-(1,2-dibromo-2-nitroethyl)-(22013-79-2)

Safety Data

• Hazardous Substances Data: 22013-79-2(Hazardous Substances Data)

Upstream product

• 101671-01-6 1-nitro-2-(4-chlorophenyl)ethylene 
• 706-07-0 1-chloro-4-(2-nitrovinyl)benzene 
• 104-88-1 4-chlorobenzaldehyde 

Downstream Products

• 22013-80-5 1-(2-bromo-2-nitrovinyl)-4-chlorobenzene 
• 18315-81-6 (Z)-2-bromo-2-nitro-1-phenylethene 
• 65185-68-4 (E)-2-bromo-β-nitrostyrene 
• 215780-07-7 Dimethyl (α-bromonitromethyl-p-chlorobenzyl)malonate 
• 59019-41-9 1-[(Z)-2-bromo-2-nitroethenyl]-4-chlorobenzene 

Relevant articles and documents

Reactions of 1-Bromo-2-(p-chlorophenyl)-1-nitroethene with CH Acids

According to 1H NMR and UV spectral data, 1-bromo-2-(p-chlorophenyl)-1-nitroethene has Z configuration. Its reactions with a series of CH acids result in formation of nucleophilic addition products (with 2-phenyl-1,3-indandione and diethyl malo

1-Bromo-2-p-chlorophenyl-1-nitroethene: Synthesis and Reactions with 1,3-Cyclohexanediones

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Research on antitumor chemotherapy: X. β Nitrostyrene and nitrovinyl derivatives

In previous work, the antitumoral cytotoxicity of β nitrostyrenes obtained by simplification of the aristolochic acid molecule was demonstrated. The effect of modifying the 3 characteristic parts of the β nitrostyrene molecule was then investigated. Results in vitro and in vivo indicate a probable mechanism of action for the β nitrostyrene and nitrovinyl compounds studied, and permit definition of the maximum simplification compatible with retention of biological activity.