7396-80-7

Basic information

• Product Name: Methanone, (2,4-dimethoxyphenyl)(2-fluorophenyl)-
• Synonyms: (2,4-dimethoxyphenyl)-(2-fluorophenyl)methanone
• CAS NO: 7396-80-7
• Molecular Formula: C15H13FO3
• Molecular Weight: 260.265
• Mol File: 7396-80-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Methanone, (2,4-dimethoxyphenyl)(2-fluorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanone, (2,4-dimethoxyphenyl)(2-fluorophenyl)-(7396-80-7)
• EPA Substance Registry System: Methanone, (2,4-dimethoxyphenyl)(2-fluorophenyl)-(7396-80-7)

Safety Data

• Hazardous Substances Data: 7396-80-7(Hazardous Substances Data)

Upstream product

• 138109-49-6 2,4-dimethoxyphenylmagnesium bromide 
• 393-52-2 2-Fluorobenzoyl chloride 
• 151-10-0 1,3-Dimethoxybenzene 
• 445-29-4 o-fluoro-benzoic acid 

Downstream Products

• 906876-74-2 N₁-phenylmethyl-5-(1,2-benzisoxazol-3-yl)-2,4-dimethoxybenzenecarboxamide 
• 906876-62-8 5-(1,2-benzisoxazol-3-yl)-2,4-dimethoxybenzenecarboxylic acid 
• 906876-38-8 5-(1,2-benzisoxazol-3-yl)-2,4-dimethoxybenzenecarboxylic acid methyl ester 
• 1279869-86-1 5-(1,2-benzoxazol-3-yl)-2,4-dimethoxybenzaldehyde 
• 906876-03-7 3-(2,4-dimethoxyphenyl)-1,2-benzisoxazole 
• 1374822-45-3 (2,4-dimethoxyphenyl)(2-morpholinophenyl)methanone 
• 906875-92-1 (2,4-dimethoxyphenyl)-{2-[(isopropylidene)amino]oxyphenyl}methanone 
• 3119-88-8 2'-fluoro-2-hydroxy-4-methoxybenzophenone 

Relevant articles and documents

Continuous flow synthesis of diaryl ketones by coupling of aryl Grignard reagents with acyl chlorides under mild conditions in the ecofriendly solvent 2-methyltetrahydrofuran

An efficient continuous flow sequential synthesis of diaryl ketones was achieved by coupling of aryl Grignard reagents with acyl chlorides in the bio-derived “green” solvent 2-methyltetrahydrofuran (2-MeTHF) under mild reaction conditions (ambient temperature, 1 hour), allowing a safe and on-demand generation of 2-(3-benzoylphenyl)propionitrile with a productivity of 3.16 g hour?1

BeCl2 as a new highly selective reagent for dealkylation of aryl-methyl ethers

An efficient and simple method is introduced for the selective removal of methyl group from poly aryl-methyl ethers, in some important derivatives of benzophenones, xanthones, anthraquinones, aryl esters, benzamides and nitroanisoles with BeCl2.