13858-69-0

Basic information

• Product Name: phenyl[5-(4-methoxyphenyl)thiophene-2-yl]methanone
• Synonyms: phenyl[5-(4-methoxyphenyl)thiophene-2-yl]methanone
• CAS NO: 13858-69-0
• Molecular Weight: 294.374
• Mol File: 13858-69-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: phenyl[5-(4-methoxyphenyl)thiophene-2-yl]methanone(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl[5-(4-methoxyphenyl)thiophene-2-yl]methanone(13858-69-0)
• EPA Substance Registry System: phenyl[5-(4-methoxyphenyl)thiophene-2-yl]methanone(13858-69-0)

Safety Data

• Hazardous Substances Data: 13858-69-0(Hazardous Substances Data)

Upstream product

• 31161-46-3 2-benzoyl-5-bromothiophene 
• 5720-07-0 4-methoxyphenylboronic acid 
• 98-88-4 benzoyl chloride 
• 130339-76-3 (5-iodo-2-thienyl)(phenyl)methanone 
• 13139-86-1 4-methoxyphenyl magnesium bromide 

Downstream Products

• 42545-43-7 2-(4-methoxyphenyl)thiophene 
• 65-85-0 benzoic acid 

Relevant articles and documents

Metal-Free Aerobic Oxidative Selective C-C Bond Cleavage in Heteroaryl-Containing Primary and Secondary Alcohols

A transition-metal-free aerobic oxidative selective C-C bond-cleavage reaction in primary and secondary heteroaryl alcohols is reported. This reaction was highly efficient and tolerated various heteroaryl alcohols, generating a carboxylic acid derivative and a neutral heteroaromatic compound. Experimental studies combined with density functional theory calculations revealed the mechanism underlying the selective C-C bond cleavage. This strategy also provides an alternative simple approach to carboxylation reaction.