52806-52-7

Basic information

• Product Name: N-(4-methoxyphenyl)-N'-phenylbenzamidine
• Synonyms: N-(4-methoxyphenyl)-N'-phenylbenzamidine
• CAS NO: 52806-52-7
• Molecular Weight: 302.376
• Mol File: 52806-52-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(4-methoxyphenyl)-N'-phenylbenzamidine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-methoxyphenyl)-N'-phenylbenzamidine(52806-52-7)
• EPA Substance Registry System: N-(4-methoxyphenyl)-N'-phenylbenzamidine(52806-52-7)

Safety Data

• Hazardous Substances Data: 52806-52-7(Hazardous Substances Data)

Upstream product

• 34918-74-6 N-(4-methoxyphenyl)benzimidoyl chloride 
• 62-53-3 aniline 
• 67-56-1 methanol 
• 53170-30-2 N-Hydroxy-N,N'-diphenylbenzamidin 
• 104-94-9 4-methoxy-aniline 
• 38430-03-4 N-phenylbenzimidoyl chloride 
• 93-98-1 N-phenyl benzoyl amide 
• 98-88-4 benzoyl chloride 
• 413576-78-0 C₂₀H₁₈N₂O*ClH 
• 7472-54-0 C₁₄H₁₃NO₂ 
• 7472-54-0 N-(p-methoxyphenyl)benzamide 

Relevant articles and documents

Synthesis, antileishmanial activity and structure-activity relationship of 1-N-X-phenyl-3-N′-Y-phenyl-benzamidines

Two series of N,N′-diphenyl-benzamidines were synthesized as part of a study to search potential new drugs with antileishmanial activity. These compounds were obtained by anilides in PCl5 halogenation reaction with generation in situ of the cor

Memory Effects and 1,3-Diazepine Ring Closure in Arylnitrenium Ions

15N- and 18O-Labelling experiments demonstrate that in the aromatic rearrangement of N,N'-diphenyl-N-(4-tosyloxy)benzamidines (2 -> 3 - 6) a strong memory effect occurs in oriented contact ion pairs.The formation of 1,3-diazepines 9 by ring closure betwee