133436-18-7

Basic information

• Product Name: (2-amino-5-methylphenyl)(4-chlorophenyl)methanone
• Synonyms: (2-amino-5-methylphenyl)(4-chlorophenyl)methanone
• CAS NO: 133436-18-7
• Molecular Weight: 245.708
• Mol File: 133436-18-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2-amino-5-methylphenyl)(4-chlorophenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (2-amino-5-methylphenyl)(4-chlorophenyl)methanone(133436-18-7)
• EPA Substance Registry System: (2-amino-5-methylphenyl)(4-chlorophenyl)methanone(133436-18-7)

Safety Data

• Hazardous Substances Data: 133436-18-7(Hazardous Substances Data)

Upstream product

• 16687-61-9 5-(4-chlorophenyl)-1H-tetrazole 
• 36360-33-5 Terephthalsaeure-bis-(p-toluidid) 
• 212200-93-6 N,N'-Bis(4-tolyl)terephthalimidoyl dichloride 
• 4692-99-3 6-methyl-1H-benzo[d][1,3]oxazine-2,4-dione 
• 2941-78-8 2-Amino-5-methylbenzoic acid 
• 106-39-8 bromochlorobenzene 
• 205756-30-5 2-amino-N-methoxy-N,5-dimethylbenzamide 
• 858788-75-7 2-(4-chlorophenyl)-5-methyl-1H-indole 

Downstream Products

• 91714-11-3 7-(4-Chloro-benzoyl)-5-methyl-1,3-dihydro-indol-2-one 
• 91714-10-2 7-(4-Chloro-benzoyl)-5-methyl-3-methylsulfanyl-1,3-dihydro-indol-2-one 
• 83388-25-4 Sodium; [2-amino-3-(4-chloro-benzoyl)-5-methyl-phenyl]-acetate 
• 1449372-92-2 3-acetyl-4-(4-chlorophenyl)-6-methylquinolin-2(1H)-one 
• 1449373-73-2 4-(4-chlorophenyl)-3-[5-(4-chlorophenyl)-4,5-dihydro-1H-pyrazol-3-yl]-6-methylquinolin-2(1H)-one 
• 1449374-18-8 4-{5-(4-chlorophenyl)-3-[4-(4-chlorophenyl)-6-methyl-2-oxo-1,2-dihydroquinolin-3-yl]-4,5-dihydro-1H-pyrazol-1-yl}-4-oxobutanoic acid 
• 1449373-28-7 (E)-4-(4-chlorophenyl)-3-[3-(4-chlorophenyl)acryloyl]-6-methylquinolin-2(1H)-one 

Relevant articles and documents

2-Arylindoles: A new entry to transition metal-free synthesis of 2-aminobenzophenones

Various 2-aminobenzophenones were synthesized from readily available 2-arylindoles in DMSO under O2 balloon atmosphere. The synthesis was carried out without the aid of a transition metal catalyst or moisture-sensitive organometallic reagents from 2-arylindoles.

Tetrazoles: XXXV. Synthesis of 3H-1,3,4-Benzotriazepines from 5-Aryltetrazoles

Reaction of 5-aryltetrazoles with N,N′-bis(p-tolyl)terephthalimidoyl dichloride under conditions of phase-transfer catalysis yields isomeric N-imidoyltetrazoles whose thermolysis results in formation of 3H-1,3,4-benzotriazepines. The latter are hydrolyzed by the action of hydrochloric acid to afford terephthalic acid and the corresponding aminobenzophenone.