22013-79-2

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

• 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 
• 22013-80-5 1-(2-bromo-2-nitrovinyl)-4-chlorobenzene 
• 59019-41-9 1-[(Z)-2-bromo-2-nitroethenyl]-4-chlorobenzene 

Relevant academic research and scientific papers

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

Aqueous isothiazolone formulation

An aqueous isothiazolone formulation useful for antiseptic or antifungal treatment of various synthetic polymeric emulsions, which comprises (a) a specific isothiazolone compound, (b) water or an aqueous solvent and (c) a specific nitrobromo or cyanobromo compound.

Insecticidal and acaricidal diarylpyrrolecarbonitrile and diarylnitropyrrole compounds

This invention relates to new diarylpyrrolecarbonitrile and new diarylnitropyrrole compounds. It also relates to the use of said compounds as insecticidal and acaricidal agents and to a method of protecting plants, particularly crop plants, from attack by

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.