272463-80-6

Basic information

• Product Name: 4-[5,7-dihydroxy-3-(4-hydroxyphenyl)-4-oxo-4H-chromen-2-yl]butanoic acid
• Synonyms: 4-[5,7-dihydroxy-3-(4-hydroxyphenyl)-4-oxo-4H-chromen-2-yl]butanoic acid
• CAS NO: 272463-80-6
• Molecular Weight: 356.332
• Mol File: 272463-80-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-[5,7-dihydroxy-3-(4-hydroxyphenyl)-4-oxo-4H-chromen-2-yl]butanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-[5,7-dihydroxy-3-(4-hydroxyphenyl)-4-oxo-4H-chromen-2-yl]butanoic acid(272463-80-6)
• EPA Substance Registry System: 4-[5,7-dihydroxy-3-(4-hydroxyphenyl)-4-oxo-4H-chromen-2-yl]butanoic acid(272463-80-6)

Safety Data

• Hazardous Substances Data: 272463-80-6(Hazardous Substances Data)

Upstream product

• 108-73-6 3,5-dihydroxyphenol 
• 14191-95-8 4-cyanomethylphenol 
• 108-55-4 glutaric anhydride, 
• 15485-65-1 2,4,4',6-tetrahydroxydeoxybenzoin 
• 5205-39-0 ethyl glutaroyl chloride 

Relevant articles and documents

Synthesis and evaluation of the antiproliferative activities of derivatives of carboxyalkyl isoflavones linked to N-t-Boc-hexylenediamine

The isoflavones biochanin A (1a), genistein (1b), and daidzein (4) at concentrations >20 μM inhibit cell growth of various cancer cell lines. To enhance the antiproliferative activities of these compounds, we synthesized three analogs, 2-[3-carboxy-(6-ter

ISOFLAVONE DERIVATIVES AND USES THEREOF

Isoflavone derivatives are provided comprising a carboxyalkylene moiety linked via its alkylene chain to the aromatic ring and via its carboxy group to an aminoalkyleneamino residue, which, in turn, is covalently linked to a functional group B. The isofla