55326-10-8

Basic information

• Product Name: Methanone, (4-methoxyphenyl)-4-quinazolinyl-
• Synonyms: Methanone,(4-methoxyphenyl)-4-quinazolinyl;(4-methoxy-phenyl)-quinazolin-4-yl-methanone
• CAS NO: 55326-10-8
• Molecular Formula: C16H12N2O2
• Molecular Weight: 264.283
• Mol File: 55326-10-8.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Methanone, (4-methoxyphenyl)-4-quinazolinyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanone, (4-methoxyphenyl)-4-quinazolinyl-(55326-10-8)
• EPA Substance Registry System: Methanone, (4-methoxyphenyl)-4-quinazolinyl-(55326-10-8)

Safety Data

• Hazardous Substances Data: 55326-10-8(Hazardous Substances Data)

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 253-82-7 quinazoline 
• 7099-91-4 p-methoxybenzoylformic acid 
• 40140-16-7 ethyl (p-methoxyphenyl)oxoacetate 
• 5257-06-7 N-(2-acetylphenyl)formamide 
• 551-93-9 2-aminoacetophenone 
• 700-46-9 4-methylquinazoline 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 187875-75-8 (4-methoxyphenyl)(1-methyl-1H-imidazol-2-yl)methanol 
• 187875-33-8 1-methyl-2-(α-hydroxy-4-methoxylbenzyl)benzimidazole 
• 1632-83-3 1-Methylbenzimidazole 
• 5190-68-1 4-chloroquinazoline 
• 98512-24-4 Benzoic acid (4-methoxy-phenyl)-quinazolin-4-yl-methyl ester 

Downstream Products

• 187336-14-7 1-(4-methoxyphenyl)-2-phenyl-1-(quinazoline-4-yl)ethanol 
• 70532-39-7 4-(4'-methoxyphenyl)quinazoline 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 253-82-7 quinazoline 
• 187336-16-9 1-(4-methoxyphenyl)-1-(quinazolin-4-yl)ethanol 
• 187336-15-8 (4-Methoxy-phenyl)-phenyl-quinazolin-4-yl-methanol 
• 100-09-4 4-methoxybenzoic acid 
• 99955-89-2 4-(4-Methoxy-phenyl)-3,4-dihydro-quinazoline-4-carboxylic acid 

Relevant articles and documents

Metal-, Photocatalyst-, and Light-Free Direct C-H Acylation and Carbamoylation of Heterocycles

Direct C-H acylations and carbamoylations of heterocycles can now be readily achieved without requiring any conventional metal, photocatalyst, electrocatalysis, or light activation, thus significantly improving on sustainability, costs, toxicity, waste, and simplicity of the operational procedure. These mild conditions are also suitable for gram-scale reactions and late-stage functionalizations of complex molecules, including pharmaceuticals, N,N-ligands, and light-sensitive molecules.

Pd(0)-catalyzed benzylic arylation-oxidation of 4-methylquinazolines via sp3 C-H activation under air conditions

An efficient and selective Pd(0)-catalyzed sp3 C-H bond arylation-oxidation of 4-methylquinazolines is reported. The method enables the introduction of arylketone at the benzylic position of 4-methylquinazolines without the use of an additional directing group, and atmospheric oxygen is used as the sole oxidant.

Catalytic action of azolium salts. IV. Preparations of 4-aroylquinazolines and 4-aroyl-1H-pyrazolo[3,4-d]pyrimidines by catalytic action of 1,3-dimethylimidazolium iodide

The ability of 1,3-dimethylimidazolium iodide (1) to catalyze the aroylation of the chloroheteroarenes 4-8 with arenecarbaldehydes 3 as sources of the aroyl groups was examined in order to develop a preparative method of aroylheteroarenes. In the presence