39923-62-1

Basic information

• Product Name: 4-hydroxy-7-methoxy-3-(3-oxo-1-phenylbutyl)benzopyran-2-one
• Synonyms: 4-hydroxy-7-methoxy-3-(3-oxo-1-phenylbutyl)benzopyran-2-one
• CAS NO: 39923-62-1
• Molecular Weight: 338.36
• Mol File: 39923-62-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-hydroxy-7-methoxy-3-(3-oxo-1-phenylbutyl)benzopyran-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 4-hydroxy-7-methoxy-3-(3-oxo-1-phenylbutyl)benzopyran-2-one(39923-62-1)
• EPA Substance Registry System: 4-hydroxy-7-methoxy-3-(3-oxo-1-phenylbutyl)benzopyran-2-one(39923-62-1)

Safety Data

• Hazardous Substances Data: 39923-62-1(Hazardous Substances Data)

Upstream product

• 17575-15-4 4-hydroxy-7-methoxycoumarine 
• 1896-62-4 (E)-benzalacetone 
• 67-56-1 methanol 
• 122-57-6 1-Phenylbut-1-en-3-one 
• 92824-14-1 4-hydroxy-5,7-dimethyl-3-(3-oxo-1-phenylbutyl)-2H-1-benzopyran-2-one 
• 552-41-0 1-(2-hydroxy-4-methoxyphenyl)ethanone 
• 89-84-9 2',4'-dihydroxy-4-acetophenone 

Relevant articles and documents

COMPOUND DIVERSIFICATION USING LATE STAGE FUNCTIONALIZATION

The present invention relates to methods for generating limited chemical diversity for biologically relevant lead molecules by late state functionalization, separation, and post-functionalization modification. The methods optionally include one or more sc

OXYGEN HETEROCYCLES BY SULPHUR YLIDE ANNULATION. IX. 3,4-DIHYDRO-2-HYDROXYMETHYL-2H,5H-PYRANOBENZOPYRAN-5-ONES FROM 3-(3-OXOALKYL)-4-HYDROXYCOUMARINS AND DIMETHYLSULPHOXONIUM METHYLIDE

Several 3-(3-oxoalkyl)-4-hydroxycoumarins have been synthesized from the corresponding 4-hydroxycoumarins and they have been reacted with dimethylsulphoxonium methylide.Transfer of one methylene group to the carbonyl function takes place and the regio- and site-selective opening of the so formed epoxide by action of the oxygen in position 4 of the coumarin moiety gives 3,4-dihydro-2-hydroxymethyl-2H,5H-pyranobenzopyran-5-ones in medium to high yields.A full spectral characterization of twenty new products has been made, and a discussion on the different factors controlling the reaction mechanism is also reported.