1616889-94-1

Basic information

• Product Name: 3-bromo-4-(5-methyl-2-methoxyphenyl)furan-2(5H)-one
• Synonyms: 3-bromo-4-(5-methyl-2-methoxyphenyl)furan-2(5H)-one
• CAS NO: 1616889-94-1
• Molecular Weight: 283.122
• Mol File: 1616889-94-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-bromo-4-(5-methyl-2-methoxyphenyl)furan-2(5H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-bromo-4-(5-methyl-2-methoxyphenyl)furan-2(5H)-one(1616889-94-1)
• EPA Substance Registry System: 3-bromo-4-(5-methyl-2-methoxyphenyl)furan-2(5H)-one(1616889-94-1)

Safety Data

• Hazardous Substances Data: 1616889-94-1(Hazardous Substances Data)

Upstream product

• 104-93-8 p-methylanizole 
• 149418-41-7 3,4-dibromo-2(5H)-furanone 
• 127972-00-3 2-methoxy-5-methylphenyl boronic acid 

Downstream Products

• 1561859-21-9 3-bromo-5-(3-chlorobenzyl)-5-hydroxy-1-isobutyl-4-(5-methyl-2-methoxyphenyl)pyrrol-2(5H)-one 
• 1561859-23-1 3-bromo-5-(2-chlorobenzyl)-5-hydroxy-1-isobutyl-4-(5-methyl-2-methoxyphenyl)pyrrol-2-(5H)-one 
• 1561859-40-2 (Z)-3-bromo-5-(3-chlorobenzylidene)-1-isobutyl-4-(5-methyl-2-methoxyphenyl)pyrrol-2(5H)-one 
• 1561859-69-5 (E)-3-bromo-5-(3-chlorobenzylidene)-1-isobutyl-4-(5-methyl-2-methoxyphenyl)pyrrol-2(5H)-one 
• 1561859-42-4 (Z)-3-bromo-5-(2-chlorobenzylidene)-1-isobutyl-4-(5-methyl-2-methoxyphenyl)pyrrol-2(5H)-one 
• 1561859-73-1 (E)-3-bromo-5-(2-chlorobenzylidene)-1-isobutyl-4-(5-methyl-2-methoxyphenyl)pyrrol-2(5H)-one 
• 1561858-97-6 (Z)-3-bromo-5-(3-chlorobenzylidene)-4-(5-methyl-2-methoxyphenyl)furan-2(5H)-one 
• 1561858-99-8 (Z)-3-bromo-5-(2-chlorobenzylidene)-4-(5-methyl-2-methoxyphenyl)furan-2(5H)-one 

Relevant articles and documents

Palladium-catalyzed hydrodehalogenation of butenolides: An efficient and sustainable access to β-arylbutenolides

Several α-unsubstituted β-arylbutenolides have been prepared in 69–92% yield by reductive dehalogenation of α-halo-β-arylbutenolides. The latter were assembled in a single-step from α,β-dihalobutenolides, which are accessible on a large-scale from biomass-derived furfural. Our dehalogenation protocol is illustrated by a new synthesis of the marine antibiotics rubrolide E and F, and 3″-bromorubrolide F.