82363-24-4

Basic information

• Product Name: (3,4-dimethoxybenzylidene)-(4-methoxyphenyl)amine
• Synonyms: (3,4-dimethoxybenzylidene)-(4-methoxyphenyl)amine
• CAS NO: 82363-24-4
• Molecular Weight: 271.316
• Mol File: 82363-24-4.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: (3,4-dimethoxybenzylidene)-(4-methoxyphenyl)amine(CAS DataBase Reference)
• NIST Chemistry Reference: (3,4-dimethoxybenzylidene)-(4-methoxyphenyl)amine(82363-24-4)
• EPA Substance Registry System: (3,4-dimethoxybenzylidene)-(4-methoxyphenyl)amine(82363-24-4)

Safety Data

• Hazardous Substances Data: 82363-24-4(Hazardous Substances Data)

Upstream product

• 104-94-9 4-methoxy-aniline 
• 93-03-8 (3,4-dimethoxyphenyl)methanol 
• 120-14-9 3,4-dimethoxy-benzaldehyde 

Downstream Products

• 5415-56-5 2-phenyl-4-veratryliden-4H-oxazol-5-one 
• 98281-45-9 <4-Methoxy-anilin>-<3,4-dimethoxy-phenyl>-essigsaeure-nitril 
• 1610556-39-2 C₂₁H₂₄ClNO₄ 
• 1610556-34-7 C₂₀H₂₅NO₃ 
• 1419351-64-6 benzyl ((E)-2-((2S,4R)-2-(3,4-dimethoxyphenyl)-6-methoxy-1,2,3,4-tetrahydroquinolin-4-yl)vinyl)carbamate 
• 1254709-08-4 (2S,3R)-tert-butyl 2-(2,6-dichlorobenzyloxy)-3-(3,4-dimethoxyphenyl)-3-(4-methoxyphenylamino) propanoate 

Relevant articles and documents

Molecular design, synthesis, and biological evaluation of bisamide derivatives as cyclophilin A inhibitors for HCV treatment

Hepatitis C virus (HCV) is a major cause of end-stage liver diseases. Direct-acting antivirals (DAAs), including inhibitors of nonstructural proteins (NS3/4A protease, NS5A, and NS5B polymerase), represent key components of anti-HCV treatment. However, so

Metal-Free Ring Opening Cyclization of Cyclopropane Carbaldehydes and N-Benzyl Anilines: An Eco-Friendly Access to Functionalized Benzo[b]azepine Derivatives

Herein, we report a p-toluenesulfonic acid (PTSA) initiated mild and user-friendly ring opening/domino ring opening cyclization reaction (depends on substituent present in N-benzyl aniline) of cyclopropane carbaldehyde and N-benzyl aniline towards the formation of substituted 4-amino butanal/2,3-dihydro-1H-benzo[b]azepine. The product dihydro-1H-benzo[b]azepine was also converted into the corresponding tetrahydro-1H-benzo[b]azepine. (Figure presented.).

Solvent-free synthesis, spectral correlations and antimicrobial activities of some aryl imines

A series of aryl imines have been synthesized by Fly-ash: H 2SO4 catalyzed microwave assisted process under solvent-free conditions. The yields of the imines have been found to be more than 87%. The purity of all imines has been checked using their physical constants and spectral data as published earlier in literature. The UV λmaxCN(nm), infrared νCN(cm-1), NMR δ(ppm) of CH and CN spectral data have been correlated with Hammett substituent constants and F and R parameters using single and multi-linear regression analysis. From the results of statistical analysis, the effect of substituents on the above spectral data has been studied. The antimicrobial activities of All synthesised imines have been studied using Bauer-Kirby method.