89523-40-0

Basic information

• Product Name: Ethanimidamide, N,N'-bis(4-methylphenyl)-N-[(4-methylphenyl)sulfonyl]-
• CAS NO: 89523-40-0
• Molecular Formula: C23H24N2O2S
• Molecular Weight: 392.522
• Mol File: 89523-40-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Ethanimidamide, N,N'-bis(4-methylphenyl)-N-[(4-methylphenyl)sulfonyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanimidamide, N,N'-bis(4-methylphenyl)-N-[(4-methylphenyl)sulfonyl]-(89523-40-0)
• EPA Substance Registry System: Ethanimidamide, N,N'-bis(4-methylphenyl)-N-[(4-methylphenyl)sulfonyl]-(89523-40-0)

Safety Data

• Hazardous Substances Data: 89523-40-0(Hazardous Substances Data)

Upstream product

• 5132-17-2 N¹,N²-Di(p-methylphenyl)acetamidine 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 599-86-0 4-methyl-N-(4-methylphenyl)benzenesulfonamide 
• 102878-71-7 2-hydroxy-N-(4-methylphenyl)acetamide 
• 129957-46-6 N-(acetoxyacetyl)-p-toluidine 
• 103-89-9 4-Methylacetanilide 
• 16634-82-5 N-(p-tolyl)-2-chloroacetamide 
• 129957-40-0 N¹-(p-Nitrobenzenesulfonyl)-N¹-(p-methylphenyl)-N²-(p-chlorophenyl)-acetamidine 
• 129957-41-1 N¹-(p-Nitrobenzenesulfonyl)-N²-(p-methylphenyl)-N¹-(p-chlorophenyl)-acetamidine 
• 129957-45-5 N¹-(p-nitrophenyl)-N²-(p-methylphenyl)-N¹-(p-chlorphenyl)acetamidine 
• 129957-44-4 N¹-(p-nitrophenyl)-N¹-(p-methylphenyl)-N²-(p-chlorphenyl)acetamidine 
• 128915-25-3 N-(2,4-Dinitro-phenyl)-N'-p-tolyl-acetamidine 
• 128915-20-8 N-(4-Nitro-phenyl)-N'-p-tolyl-acetamidine 
• 129957-39-7 N-(4-Chloro-phenyl)-N'-p-tolyl-acetamidine 
• 64309-77-9 N-tosyl-p-toluidine sodium salt 
• 129957-33-1 N¹-Tosyl-N¹-(p-methoxyphenyl)-N²-(p-methylphenyl)acetamidine 

Relevant articles and documents

Hydrolysis of Acyl Derivatives of N1,N2-Diarylamidine. I

The alkaline hydrolyses of N1-benzoyl-N1,N2-diarylacetamidine (V) and N1-tosyl-N1,N2-diarylacetamidine (IX) were examined.In the hydrolysis of V, hydroxide ion attacked the amide carbonyl carbon to form N1,N2-diarylacetamidine and benzoic acid.In the hydrolysis of IX, hydroxide ion attacked the amidine carbon, and elimination of the N-tosylarylamino group and arylimino group proceeded in parallel, with that of the latter predominating.The alcoholysis reaction of V proceeded without any added catalyst, in contrast to the case of 1-(N-benzoylarylamino)-3-arylimino-1-propene.A unique peak corresponding to the loss of 64 mass units (sulfur dioxide) was observed in the mass spectrum of IX.Keywords - alkaline hydrolysis; alcoholysis; N1-benzoyl-N1,N2-diarylacetamidine; N1-tosyl-N1,N2-diarylacetamidine; 1,1-bis(N-benzoylarylamino)ethene; MS