6454-01-9

Basic information

• Product Name: Methanone, 3-benzofuranylphenyl-
• Synonyms: Methanone,3-benzofuranylphenyl
• CAS NO: 6454-01-9
• Molecular Formula: C15H10O2
• Molecular Weight: 222.243
• Mol File: 6454-01-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Methanone, 3-benzofuranylphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanone, 3-benzofuranylphenyl-(6454-01-9)
• EPA Substance Registry System: Methanone, 3-benzofuranylphenyl-(6454-01-9)

Safety Data

• Hazardous Substances Data: 6454-01-9(Hazardous Substances Data)

Upstream product

• 55877-31-1 benzofuran-3-carbonitrile 
• 1192031-31-4 ethoxycarbonylmethyl 2-(2'-phenylethynyl)phenyl ether 
• 59214-70-9 3-bromobenzofuran 
• 113180-51-1 [2-(2-Oxo-2-phenyl-acetyl)-phenoxy]-acetic acid 
• 34589-99-6 2-hydroxybenzil 
• 34082-43-4 2-methoxybenzil 
• 854630-15-2 2-(2-methoxyphenyl)-3-oxo-3-phenylpropanal 

Downstream Products

• 68218-56-4 3-(2-phenylbenzofuran-3-yl)propanoic acid 
• 1131341-95-1 3-(2-phenylbenzofuran-3-yl)propionic acid ethyl ester 
• 1131341-92-8 3-(2-phenylbenzofuran-3-yl)propanenitrile 
• 37883-65-1 2-(2-hydroxyphenyl)-1-phenylethan-1-one 
• 1244029-96-6 tert-butyl 3-(2-phenylbenzofuran-3-yl)propanoate 
• 92497-79-5 2-(5-phenyl-isoxazol-4-yl)-phenol 

Relevant articles and documents

Synthesis of carbonylated heteroaromatic compounds: Via visible-light-driven intramolecular decarboxylative cyclization of o -alkynylated carboxylic acids

An efficient strategy for the easy access to carbonylated heteroaromatic compounds has been developed via a visible-light-promoted intramolecular decarboxylative cyclization reaction of o-alkynylated carboxylic acids. This method is characterized by its b

Intramolecular Ketene Cycloadditions. Synthesis of Isoflavones and 3-Aroylbenzofurans

The conversion of 2-(carboxyalkoxy)benzils to the corresponding phenoxyketenes to an intramolecular ketene cycloaddition to ultimately yield isoflavones and/or 3-aroylbenzofurans.The ketenes may be generated by the classical dehydrochlorination of the acid chloride or by using Perkin reaction conditions, sodium acetate in refluxing acetic anhydride.The initial cycloaddition products are the corresponding β-lactones, which may decarboxylate to the isolated isoflavones and/or 2-aroylbenzofurans.The product distributions are dependent upon the substitution pattern in the orginal benzil acids.