60112-48-3

Basic information

• Product Name: 2(3H)-Furanone, 5-(4-bromophenyl)-
• CAS NO: 60112-48-3
• Molecular Formula: C10H7BrO2
• Molecular Weight: 239.068
• Mol File: 60112-48-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2(3H)-Furanone, 5-(4-bromophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2(3H)-Furanone, 5-(4-bromophenyl)-(60112-48-3)
• EPA Substance Registry System: 2(3H)-Furanone, 5-(4-bromophenyl)-(60112-48-3)

Safety Data

• Hazardous Substances Data: 60112-48-3(Hazardous Substances Data)

Upstream product

• 20005-42-9 5-(4-bromophenyl)-2-furancarboxyaldehyde 
• 85060-86-2 2,2-dimethyl-5-(p-bromophenacyl)-1,3-dioxane-4,6-dione 
• 6340-79-0 4-oxo-4-(4-bromophenyl)butanoic acid 

Relevant articles and documents

A Piperine-Based Scaffold as a Novel Starting Point to Develop Inhibitors against the Potent Molecular Target OfChtI

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A facile synthesis of γ-butenolides via cyclization of 3-alkenoic acids with dimethyl sulfoxide and oxalyl bromide

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Catalytic osmium-assisted oxidative cleavage of olefins

An osmium-assisted process for the oxidative cleavage of oxidizable organic compounds such as unsaturated organic compounds, including alkenes and olefins into aldehydes, carboxylic acids, esters, or ketones. The process uses a metal catalyst comprising osmium and a peroxy compound selected from the group consisting of peroxymonosulfuric acid and salts thereof to oxidatively cleave the oxidizable organic compound. In particular, the process enables aldehydes, carboxylic acids, esters, or ketones to be selectively produced from the corresponding mono-, 1,1-di-, 1,2-di-, tri-, or tetra-substituted olefins in a reaction that produces the result of ozonolysis but with fewer problems. The present invention further provides a process for oxidizing an aldehyde alone or with the osmium in an interactive solvent to produce an ester or carboxylic acid.