2958-39-6

Upstream product

• 555-21-5 4-Nitrophenylacetonitrile 
• 120-14-9 3,4-dimethoxy-benzaldehyde 

Downstream Products

• 1346463-76-0 2,3-dimethoxy-6-(4-nitrophenyl)naphthalene 
• 1346463-75-9 3-(3,4-dimethoxyphenyl)-4-(4-nitrophenyl)pyridin-2(1H)-one 
• 1346463-33-9 (E)-2-(4-nitrophenyl)-3-(3,4-dimethoxyphenyl)acrylaldehyde 
• 1346463-46-4 5-(3,4-dimethoxyphenyl)-4-(4-nitrophenyl)penta-(2E,4Z)-dienoic acid 
• 1346463-60-2 5-(3,4-dimethoxyphenyl)-4-(4-nitrophenyl)penta-(2E,4Z)-dienoyl azide 
• 112890-59-2 Ethyl 2-cyano-5-(3,4-dimethoxyphenyl)-2-(p-nitrophenyl)-2,5-dihydrofuran-4-carboxylate 
• 112890-58-1 Ethyl 2-cyano-5-(3,4-dimethoxyphenyl)-2-(p-nitrophenyl)-2,5-dihydrofuran-3-carboxylate 
• 112890-62-7 Methyl 2-cyano-5-(3,4-dimethoxyphenyl)-2-(p-nitrophenyl)tetrahydrofuran-3-carboxylate 
• 112890-63-8 Methyl 2-cyano-5-(3,4-dimethoxyphenyl)-2-(p-nitrophenyl)tetrahydrofuran-4-carboxylate 
• 112890-50-3 (2S,3R)-3-(3,4-Dimethoxy-phenyl)-2-(4-nitro-phenyl)-oxirane-2-carbonitrile 

Relevant academic research and scientific papers

Isostructural polymorphs: Qualitative insights from energy frameworks

Three isostructural polymorphs with two-dimensional and three-dimensional similarities are demonstrated quantitatively from similarity relationship analysis. The similarity dimensions are then visualized and correlated in a novel way via qualitative analy

Stereoselective synthesis of Z-acrylonitrile derivatives: Catalytic and acetylcholinesterase inhibition studies

In the present study, a focused library of (Z)-acrylonitrile analogues (library A & B) were synthesized, which were typically accessed via a facile Knoevenagel condensation between p-nitrophenylacetonitrile and appropriately substituted aromatic aldehydes

Substituent effects on the iodine-catalyzed thermal cyclization of 3,4-diphenylbuta-1,3-dienyl isocyanates: Mechanistic studies

The thermal cyclization of 3,4-diphenylbuta-1,3-dienyl isocyanates 1, generated in situ from the corresponding azides, was investigated using iodine as a catalyst. Diphenylpyridinones 2, phenylnaphthalenes 3, and indenes 4 were produced via intramolecular ring closure. The nature of the substituents on the phenyl rings was found to be crucial to the distribution of cyclized products 2 - 4. The mechanism of the reaction is also discussed.