51282-12-3

Basic information

• Product Name: 2(5H)-Furanone, 5-[(3,4-dihydroxyphenyl)methylene]-4-hydroxy-3-(4-hydroxyphenyl)-
• CAS NO: 51282-12-3
• Molecular Formula: C17H12O6
• Molecular Weight: 312.279
• Mol File: 51282-12-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2(5H)-Furanone, 5-[(3,4-dihydroxyphenyl)methylene]-4-hydroxy-3-(4-hydroxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2(5H)-Furanone, 5-[(3,4-dihydroxyphenyl)methylene]-4-hydroxy-3-(4-hydroxyphenyl)-(51282-12-3)
• EPA Substance Registry System: 2(5H)-Furanone, 5-[(3,4-dihydroxyphenyl)methylene]-4-hydroxy-3-(4-hydroxyphenyl)-(51282-12-3)

Safety Data

• Hazardous Substances Data: 51282-12-3(Hazardous Substances Data)

Upstream product

• 93831-19-7 3',4',4-tribenzyloxypulvinone 
• 6547-53-1 2-[4-(benzyloxy)benzyl]acetic acid 
• 68641-16-7 (4-benzyloxy-phenyl)-acetic acid methyl ester 
• 116429-31-3 5-Bromo-5-(3,4-dimethoxy-benzyl)-4-methoxy-3-(4-methoxy-phenyl)-5H-furan-2-one 
• 116429-30-2 5-(3',4'-dimethoxyphenyl)methyl-4-methoxy-3-(4''-methoxyphenyl)furan-2(5H)-one 
• 116429-29-9 5-(3',4'-dimethoxyphenyl)methyl-4-hydroxy-3-(4''-methoxyphenyl)furan-2(5H)-one 
• 106942-15-8 4-(3',4'-dimethoxyphenyl)-3-hydroxy-1-(4''-metoxyphenyl)butan-2-one 
• 106942-20-5 3,4-dimethoxy-<(trimethylsilyl)oxy>-benzenepropanenitrile 
• 5703-21-9 3,4-dimethoxyphenylacetaldehyde 
• 71851-34-8 5-(3',4'-dimethoxyphenyl)methylene-4-methoxy-3-(4''-methoxyphenyl)furan-2(5H)-one 
• 139-85-5 3,4-dihydroxybenzaldehyde 
• 93831-20-0 (2E,4Z)-2-(4-Benzyloxy-phenyl)-5-(3,4-bis-benzyloxy-phenyl)-3,4-dihydroxy-penta-2,4-dienoic acid 
• 93831-18-6 (Z)-5'-(3,4-dibenzyloxybenzylidene)cyclohexanespiro-2'-(1',3'-dioxolan)-4'-one 
• 5447-02-9 3,4-dibenzyloxybenzaldehyde 

Downstream Products

• 71851-34-8 5-(3',4'-dimethoxyphenyl)methylene-4-methoxy-3-(4''-methoxyphenyl)furan-2(5H)-one 

Relevant articles and documents

Pigments of Fungi. XV An Efficient, Unambiguous Route to Unsymmetrically Substituted Dibenzyl Acyloins and their Use in the Synthesis of Fungus Pigments of the Pulvinone and Grevillin Types

Dibenzyl acyloins including those bearing unsymetrically disposed aryl residues are assembled in high yield by reaction between the O-trimethylsilyl ethers of arylacetaldehyde cyanohydrins and benzyl Grignard reagents.These acyloins are deprotonated with