38436-36-1

Upstream product

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

Downstream Products

• 175789-75-0 1-methyl-5-phenyl-1H-1,2,3-triazole-4-carbonitrile 
• 1217607-96-9 3-benzoyl-1-nitro-2-phenyl-1,2,3,10b-tetrahydropyrrolo[2,1-a]isoquinoline-1-carbonitrile 
• 60214-24-6 3-anilino-2-nitro-3-phenyl-propionitrile 
• 38570-10-4 4-cyano-1,3,5-triphenyl-1,5-dihydro-pyrrole-2,2-dicarboxylic acid dimethyl ester 
• 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 
• 95642-41-4 3-Nitro-2-amino-4-phenyl-7,7-dimethyl-4H,6H,8H-chromen-5-one 
• 247074-44-8 2-amino-3-nitro-4-phenyl-4,6,7,8-tetrahydro-chromen-5-one 
• 50640-06-7 1,4-diphenyl-1H-1,2,3-triazole-5-carboxylic acid 
• 4900-34-9 1,5-diphenyl-1H-1,2,3-triazole-4-carboxylic acid 
• 1309930-01-5 1-(4-methylphenyl)-4-phenyl-1H-1,2,3-triazole-5-carboxylic acid 
• 1017415-39-2 1-(4-methylphenyl)-5-phenyl-1H-1,2,3-triazole-4-carboxylic acid 

Relevant academic research and scientific papers

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

New stable form of nitroacetonitrile

Oxidation of ethyl cyanoglyoxylate 2-oxime followed by KOH treatment affords stable potassium salt of nitroacetonitrile which is a reliable substitute of hazardous free nitroacetonitrile in organic synthesis.

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

Uncatalyzed and solvent-free multicomponent process for the synthesis of biphenyl-2-carbonitrile derivatives

(Diagram presented) An innovative route to prepare a number of variously substituted new biphenyl derivatives is presented here. The protocol avoids the use of a catalyst, an organic solvent, and dry conditions.

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