73861-02-6

Basic information

• Product Name: 3-{[(4-chlorophenyl)methylene]amino}-2-phenylquinazolin-4(3H)-one
• Synonyms: 3-{[(4-chlorophenyl)methylene]amino}-2-phenylquinazolin-4(3H)-one
• CAS NO: 73861-02-6
• Molecular Weight: 359.815
• Mol File: 73861-02-6.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 3-{[(4-chlorophenyl)methylene]amino}-2-phenylquinazolin-4(3H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-{[(4-chlorophenyl)methylene]amino}-2-phenylquinazolin-4(3H)-one(73861-02-6)
• EPA Substance Registry System: 3-{[(4-chlorophenyl)methylene]amino}-2-phenylquinazolin-4(3H)-one(73861-02-6)

Safety Data

• Hazardous Substances Data: 73861-02-6(Hazardous Substances Data)

Upstream product

• 7510-49-8 methyl 2-(benzamido)benzoate 
• 134-20-3 2-carbomethoxyaniline 
• 118-92-3 anthranilic acid 
• 98-88-4 benzoyl chloride 
• 1022-46-4 2-phenyl-4H-3,1-benzoxazin-4-one 
• 1904-60-5 3-amino-2-phenylquinazolin-4(3H)-one 
• 104-88-1 4-chlorobenzaldehyde 

Downstream Products

• 623-03-0 4-Cyanochlorobenzene 
• 1022-45-3 2-phenyl-4(3H)-quinazolinone 
• 1192363-96-4 C₂₅H₁₈ClN₃O₄S 
• 106873-17-0 3-[2-(4-Chloro-phenyl)-4-oxo-thiazolidin-3-yl]-2-phenyl-3H-quinazolin-4-one 

Relevant articles and documents

Synthesis, Antimicrobial and Anticancer Evaluation of 2-Azetidinones Clubbed with Quinazolinone

A novel series of 2-azetidinones clubbed with quinazolinone was synthesized using anthranilic acid. All the synthesized compounds were evaluated for their antimicrobial activity against two Gram positive bacterial strains (Bacillus subtilis and Staphyloco

Synthesis, antiviral activity and cytotoxicity evaluation of Schiff bases of some 2-phenyl quinazoline-4(3)H-ones

A new series of 3-(benzylideneamino)-2-phenylquinazoline-4(3H)-ones were prepared through Schiff base formation of 3-amino-2-phenyl quinazoline-4(3)H-one with various substituted carbonyl compounds. Their chemical structures were elucidated by spectral st

Antibacterial activity of some 3-(arylideneamino)-2-phenylquinazoline-4(3H) -ones: Synthesis and preliminary QSAR studies

Synthesis of ten 3-(arylideneamino)-2-phenylquinazoline-4(3H)-ones is reported. All the compounds contained a common phenyl group at the 2-position, while the substituents on the arylideneamino group were varied. The compounds were investigated for their