37630-63-0

Upstream product

• 13218-13-8 nitroacetonitrile 
• 100-52-7 benzaldehyde 

Downstream Products

• 38570-10-4 4-cyano-1,3,5-triphenyl-1,5-dihydro-pyrrole-2,2-dicarboxylic acid dimethyl ester 
• 247074-44-8 2-amino-3-nitro-4-phenyl-4,6,7,8-tetrahydro-chromen-5-one 
• 95642-41-4 3-Nitro-2-amino-4-phenyl-7,7-dimethyl-4H,6H,8H-chromen-5-one 
• 17529-01-0 1-phenyl-2,3-diaza-4-(9-fluorenylidene)buta-1,3-diene 
• 14677-11-3 4-phenyl-1H-1,2,3-triazole-5-carbonitrile 
• 60214-24-6 3-anilino-2-nitro-3-phenyl-propionitrile 

Relevant academic research and scientific papers

Aryl(hetaryl)-containing gem-cyanonitroethenes: Synthesis, structure, and reactions with 2,3-dimethyl-1,3-butadiene

Methods of aryl(hetaryl)-substituted gem-cyanonitroethenes preparation are summarized, and the products structure elucidation by means of 1H, 13C NMR, IR, and UV spectroscopy methods is discussed. E-Configuration of the compounds obt

Novel synthesis scheme and in vitro antimicrobial evaluation of a panel of (E)-2-aryl-1-cyano-1-nitroethenes

Drug resistance has become a major concern in the field of infection management, therefore searching for new antibacterial agents is getting more challenging. Our study presents an optimized and eco-friendly synthesis scheme for a panel of nitroalkenes be

Cycloadditions dipolaires 1,3 aux derives nitres α ethyleniques, acetyleniques potentiels. I. Reaction avec des ylures d'azomethine. Orientation et stereochimie de la cycloaddition

The stereochemistry of the nitroolefins 1 prepared by known methods was unambigously established.Their reactions with azomethine ylides (e.g. 8) was studied and the stereochemistry of the adducts as well.This preliminary work was necessary to substantiate a discussion of structural (pyrrolidines conformational analysis) and mechanistic problems (dipolarophile-azomethine ylide approach and HNO2 elimination from the nitro pyrrolidines).

PREPARATION AND Z-E ISOMERIZATION OF SUBSTITUTED NITROSTYRENES

This study concerns the synthesis of β-substituted β-nitrostyrenes by two procedures: addition of nitryl halogenides to double bonds, connected with the elimination of hydrogen halide, and condensation of aldehydes with substituted nitromethanes, and it c