150436-37-6

Basic information

• Product Name: 4H-1-Benzopyran-4-one, 2,3-dihydro-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-
• CAS NO: 150436-37-6
• Molecular Formula: C16H14O5
• Molecular Weight: 286.284
• Mol File: 150436-37-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4H-1-Benzopyran-4-one, 2,3-dihydro-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 4H-1-Benzopyran-4-one, 2,3-dihydro-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-(150436-37-6)
• EPA Substance Registry System: 4H-1-Benzopyran-4-one, 2,3-dihydro-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-(150436-37-6)

Safety Data

• Hazardous Substances Data: 150436-37-6(Hazardous Substances Data)

Upstream product

• 699-83-2 2,6-dihydroxylacetophenone 
• 5779-98-6 O-methoxymethylisovanillin 
• 78646-28-3 2′-hydroxy-6′-methoxymethoxyacetophenone 
• 3886-19-9 1-[2',6'-bis(phenylmethoxy)phenyl]ethanone 
• 76799-16-1 2,3',6,-tris(benzyloxy)-4'-methoxychalcone 
• 80693-50-1 3,2',6'-trihydroxy-4-methoxychalkone 
• 621-59-0 isovanillin 

Downstream Products

• 1449417-52-0 (R)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)chroman-4-one 
• 70412-87-2 (S)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)chroman-4-one 

Relevant articles and documents

Use of flavone and flavanone derivatives in preparation of sedative and hypnotic drugs

Disclosed is a use of flavones derivatives and flavanone derivatives in preparation of sedative and hypnotic drugs.

COMPOUNDS, COMPOSITIONS, AND METHODS FOR MODULATING SWEET TASTE

The present invention provides edible compositions comprising a sweet taste modulator of the present invention, food products comprising such edible compositions and methods of preparing such food products. The present invention also provides methods of reducing the amount of sugar in a food product, methods of reducing the caloric intake in a diet, and methods of enhancing sweet taste in a food product.

A Simple Synthesis of 5,3'-Dihydroxy-4'-methoxyflavanone

The title flavanone has now been synthesized in two steps: (i) condensation of 2-acetylresorcinol and isovanillin in the presence of aq. ethanolic potassium hydroxide affords 3,2',6'-trihydroxy-4-methoxychalkone; (ii) cyclization of the resulting chalkone