195066-98-9

Basic information

• Product Name: 2-(p-chlorobenzoyl)-5-chlorobenzophenone
• Synonyms: 2-(p-chlorobenzoyl)-5-chlorobenzophenone
• CAS NO: 195066-98-9
• Molecular Weight: 370.235
• Mol File: 195066-98-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-(p-chlorobenzoyl)-5-chlorobenzophenone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(p-chlorobenzoyl)-5-chlorobenzophenone(195066-98-9)
• EPA Substance Registry System: 2-(p-chlorobenzoyl)-5-chlorobenzophenone(195066-98-9)

Safety Data

• Hazardous Substances Data: 195066-98-9(Hazardous Substances Data)

Upstream product

• 122-01-0 4-chloro-benzoyl chloride 
• 719-59-5 5-chloro-2-aminobenzophenone 
• 719-64-2 5-chloro-3-phenylanthranil 
• 71-43-2 benzene 
• 74-11-3 para-chlorobenzoic acid 
• 118-48-9 isatoic anhydride 
• 4743-17-3 5-Chloroisatoic anhydride 

Downstream Products

• 128889-33-8 6-Amino-2-(p-aminophenyl)-4-phenylquinazoline 
• 49797-11-7 6-chloro-2(4-chloro-phenyl)-4-phenyl-quinazoline 

Relevant articles and documents

Potential plant growth regulators: Synthesis and activity of new substituted N-(2-benzoyl-4-chlorophenyl)benzamides and N-[4-chloro-2-(α, α-hydroxyphenylmethyl)phenyl]benzamides

2-Amino-5-chlorobenzophenone 3 prepared in 2 steps from isatoic anhydride 1 on condensation with substituted benzoyl chlorides 6a-i in presence of Et 3N in 1,2-dichloroethane (DCE) affords substituted N-(2-benzoyl-4-chlorophenyl)-benzamides 7a-i which on reduction with NaBH 4 gives corresponding alcohols, N-[4-chloro-2-(α,α- hydroxyphenyl-methyl)phenyl]benzamides 8a-i. The structures of all the compounds are confirmed by 1H NMR spectra, and their cytokinin (plant growth promoting) activity is determined on seeds of Raphanus sativus, family Brassicaceae (common name white radish, variety Pusa Chetki), for concentrations varying between 0.1 to 10 mg/litre. Compounds 7c, 7d, 7g and 7h at all concentrations and 7i at 4 concentrations have been found to show higher plant growth promoting (PGP) activity than benzyladenine (standard). Compounds 8d and 8g also show moderate plant growth promoting (cytokinin) activity, while compounds 7a, 7b, 7e, 7f and 8a, 8b, 8c, 8e, 8f and 8i are found to have plant growth inhibiting (PGI) activity.