22365-62-4

Basic information

• Product Name: N1,N2-Bis(p-chlorophenyl)acetamidine
• Synonyms: N1,N2-Bis(p-chlorophenyl)acetamidine
• CAS NO: 22365-62-4
• Molecular Formula: C₁₄H₁₂Cl₂N₂
• Molecular Weight: 279.1645
• Mol File: 22365-62-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 422.6°Cat760mmHg
• Flash Point: 209.4°C
• Appearance: /
• Density: 1.22g/cm³
• CAS DataBase Reference: N1,N2-Bis(p-chlorophenyl)acetamidine(CAS DataBase Reference)
• NIST Chemistry Reference: N1,N2-Bis(p-chlorophenyl)acetamidine(22365-62-4)
• EPA Substance Registry System: N1,N2-Bis(p-chlorophenyl)acetamidine(22365-62-4)

Safety Data

• Hazardous Substances Data: 22365-62-4(Hazardous Substances Data)

Upstream product

• 128799-74-6 N¹-(p-Chlorobenzoyl)-N¹,N²-di-(p-chlorophenyl)-acetamidine 
• 72535-68-3 ethyl N-(p-methoxyphenyl)acetimidate 
• 106-47-8 4-chloro-aniline 
• 26431-34-5 Ethyl N-(p-chlorophenyl)acetimidate 
• 104-94-9 4-methoxy-aniline 

Downstream Products

• 89523-38-6 N¹-benzoyl-N¹,N²-bis(p-chlorophenyl)acetamidine 
• 128799-74-6 N¹-(p-Chlorobenzoyl)-N¹,N²-di-(p-chlorophenyl)-acetamidine 
• 129957-30-8 N¹-(p-chlorobenzenesulfonyl)-N¹,N²-di(p-chlorophenyl)acetamidine 
• 32324-06-4 N¹-tosyl-N¹,N²-bis(p-chlorophenyl)acetamidine 
• 129957-35-3 N¹-(p-Nitrobenzenesulfonyl)-N¹,N²-di(p-chlorphenyl)acetamidine 
• 38756-10-4 4-methoxyphenylamino-(1,3-dioxo-2,3-dihydro-1H-inden-2-ylidene)ethanenitrile 
• 59959-74-9 (Z)-2-((4-chlorophenyl)amino)-1,4-diphenylbut-2-ene-1,4-dione 
• 89523-44-4 1,1-bisethene 
• 129957-37-5 N¹-(p-Nitrophenyl)-N¹,N²-di(p-chlorophenyl)acetamidine 
• 175406-05-0 GaCl₃*ClC₆H₄NHC(CH₃)NC₆H₄Cl 
• 175406-07-2 GaCl₂⁽¹⁺⁾*C₆H₄ClNC(CH₃)NC₆H₄Cl^(1-) = [GaCl₂][C₆H₄ClNC(CH₃)NC₆H₄Cl] 
• 1426097-49-5 6-chloro-1-(4-chlorophenyl)-2-methyl-1H-benzo[d]imidazole 

Relevant articles and documents

Organometallic complexes of aluminium, gallium and indium

Novel organometallic complexes of aluminium, gallium and indium are disclosed, having improved stability and volatility for use in CVD processes. These are donor ligand complexes of the formula MR2 L where M is the metal, R is an alkyl group and L is a ligand containing an amidine (R'N. . . C(R'). . . NR') group, where R' is H, alkyl etc.

Amidines. I. Hydrolysis of N1-acyl- and N1-tosyl-N1,N2-diarylamidines

In acid hydrolysis of N1-acyl-N1,N2-diarylamidines, a water molecule attacked exclusively the amidine central carbon, and the reaction proceeded in parallel through two pathways. One of them leads to the formation of two N-acylarylamines, and the other leads to the formation of N,N-diacylarylamine and arylamine. Acid hydrolysis of N1-tosyl-N1,N2-diarylamidine was also examined. The results were similar to those of the hydrolysis of N1-acyl-N1,N2-diarylamidines. Alkaline hydrolysis and alcoholysis of N1-acyl-N1,N2-diarylamidines occurred almost exclusively at the amide carbonyl group to give N1,N2-diarylamidines and carboxylic acids or their esters. The effects of structural change and the aryl substituents on the rate and direction of the reaction were examined.