1310486-61-3

Basic information

• Product Name: 1-(3,4-dimethoxybenzylidene)-2-benzyl-2-(4-chlorophenyl)hydrazine
• Synonyms: 1-(3,4-dimethoxybenzylidene)-2-benzyl-2-(4-chlorophenyl)hydrazine
• CAS NO: 1310486-61-3
• Molecular Weight: 380.874
• Mol File: 1310486-61-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(3,4-dimethoxybenzylidene)-2-benzyl-2-(4-chlorophenyl)hydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3,4-dimethoxybenzylidene)-2-benzyl-2-(4-chlorophenyl)hydrazine(1310486-61-3)
• EPA Substance Registry System: 1-(3,4-dimethoxybenzylidene)-2-benzyl-2-(4-chlorophenyl)hydrazine(1310486-61-3)

Safety Data

• Hazardous Substances Data: 1310486-61-3(Hazardous Substances Data)

Upstream product

• 380340-95-4 C₁₅H₁₅ClN₂O₂ 
• 100-39-0 benzyl bromide 
• 106-47-8 4-chloro-aniline 
• 1073-70-7 4-chlorophenylhydrazine hydrochloride 

Downstream Products

• 53703-86-9 1-benzyl-5-chloro-2-(3,4-dimethoxyphenyl)-1H-benzo[d]imidazole 

Relevant articles and documents

Copper-mediated synthesis of substituted 2-aryl-N-benzylbenzimidazoles and 2-arylbenzoxazoles via C-H functionalization/C-N/C-O bond formation

An efficient method for the transformation of N-benzyl bisarylhydrazones and bisaryloxime ethers to functionalized 2-aryl-N-benzylbenzimidazoles and 2-arylbenzoxazoles is described. The protocol involves a copper(II)-mediated cascade C-H functionalization/C-N/C-O bond formation under neutral conditions. Substrates having either electron-donating or -withdrawing substituents undergo the cyclization to afford the target heterocycles at moderate temperature.