55174-52-2

Basic information

• Product Name: 4,N-dimethyl-benzimidoyl chloride
• Synonyms: 4,N-dimethyl-benzimidoyl chloride
• CAS NO: 55174-52-2
• Molecular Weight: 167.638
• Mol File: 55174-52-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4,N-dimethyl-benzimidoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 4,N-dimethyl-benzimidoyl chloride(55174-52-2)
• EPA Substance Registry System: 4,N-dimethyl-benzimidoyl chloride(55174-52-2)

Safety Data

• Hazardous Substances Data: 55174-52-2(Hazardous Substances Data)

Upstream product

• 18370-11-1 N-methyl-p-methylbenzamide 

Downstream Products

• 68826-33-5 1-methyl-5-(4-methylphenyl)-1H-tetrazole 
• 74030-74-3 3,5-dimethyl-2-phenyl-6-p-tolyl-3,5-dihydro-4λ⁴-[1,2,4]thiadiazolo[5,1-e][1,2,4]thiadiazole 
• 97661-71-7 N-methyl-4-methyl-N-nitrobenzamide 
• 97661-69-3 N,4-dimethyl-N-nitrosobenzamide 
• 151328-43-7 N¹,N¹,N²,4-Tetramethylbenzamidin 
• 33369-52-7 methyl 1-Methyl-5-(4-methylbenzoyl)-1H-pyrrole-2-acetate 
• 87937-75-5 Methyl 1,4-Dimethyl-5-[(methylimino)(4-methylphenyl)methyl]-1H-pyrrole-2-acetate Perchlorate 
• 1365547-17-6 1,3,4-trimethyl-5-(4-methylphenyl)-1,4-dihydroimidazo[4,5-c]pyrazole 
• 1365546-83-3 N'-(4-bromo-1,3-dimethyl-1H-pyrazol-5-yl)-N,4-dimethylbenzimidamide 
• 1365546-66-2 N'-(1,3-dimethyl-1H-pyrazol-5-yl)-N,4-dimethylbenzimidamide 
• 87937-83-5 Methyl 1-Methyl-5[(methylimino)(4-methylphenyl)methyl]-1H-pyrrole-2-acetate Perchlorate 
• 911125-25-2 C₁₄H₁₅N 
• 87937-82-4 (1-Methyl-5-{[(E)-methylimino]-p-tolyl-methyl}-1H-pyrrol-2-yl)-acetic acid methyl ester 
• 87937-74-4 (1,4-Dimethyl-5-{[(E)-methylimino]-p-tolyl-methyl}-1H-pyrrol-2-yl)-acetic acid methyl ester 

Relevant articles and documents

Imidoyl substituted pyrroles

Novel compounds, which are aryl-pyrrolyl-imine derivatives of the Formula I STR1 and acid addition salts thereof are disclosed; which compounds may be prepared by the acid catalyzed condensation of an imidoyl chloride with a lower alkyl pyrrole-2-acetate; and which compounds are useful as intermediates to form by hydrolysis, the known useful ketone analogs which have anti-inflammatory and analgesic activity; and certain of which compounds have antisecretory, anti-irritable bowel, antidiarrheal and general behavior effect on the CNS properties.