947408-91-5

Basic information

• Product Name: 2H-1-Benzopyran-2-one, 6-(2,4-dihydroxybenzoyl)-
• Synonyms: 6-(2,4-Dihydroxybenzoyl)-2H-chromen-2-one
• CAS NO: 947408-91-5
• Molecular Formula: C16H10O5
• Molecular Weight: 282.252
• Mol File: 947408-91-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2H-1-Benzopyran-2-one, 6-(2,4-dihydroxybenzoyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-1-Benzopyran-2-one, 6-(2,4-dihydroxybenzoyl)-(947408-91-5)
• EPA Substance Registry System: 2H-1-Benzopyran-2-one, 6-(2,4-dihydroxybenzoyl)-(947408-91-5)

Safety Data

• Hazardous Substances Data: 947408-91-5(Hazardous Substances Data)

Upstream product

• 7734-80-7 2-oxo-2H-benzopyran-6-carboxylic acid 
• 151-10-0 1,3-Dimethoxybenzene 
• 947408-90-4 6-(2,4-dimethoxybenzoyl)chromen-2-one 

Downstream Products

• 947408-93-7 6-(2-hydroxy-4-cyclopentyloxybenzoyl)coumarin 
• 530141-60-7 methyl 3-[2-hydroxy-5-(2-hydroxy-4-cyclopentyloxybenzoyl)phenyl]propionate 
• 947409-01-0 methyl 3-[2-[(2-trityl-3-keto-benzisoxazol-6-yl)methoxy]-5-(2-hydroxy-4-cyclopentyloxybenzoyl)phenyl]propionate 

Relevant articles and documents

Highly efficient and scalable process for demethylation of 6-(2,4-dimethoxybenzoyl)chromen-2-one and other aryl methyl ethers

Demethylation of 6-(2,4-dimethoxybenzoyl)chromen-2-one and some other aryl methyl ethers was achieved with pyridinium bromide as demethylating agent and sulfolane as solvent. Compared with other demethylation methods, this combination offers advantages of clean conversion, excellent yields, easy operation and workup, and manageable reaction temperatures. This process could be particularly useful for large-scale production because it avoids use of corrosive or moisture-sensitive reagents. Copyright

PROCESS FOR PRODUCTION OF 3-[5-[4-(CYCLOPENTYLOXY)-2-HYDROXYBENZOYL]-2-[(3-HYDROXY-1,2-BEZISOXAZOL-6-YL)METHOXY]PHENYL]PROPIONATE ESTER AND INTERMEDIATE FOR THE PROCESS

A preparation method using as an intermediate 6-(halomethyl)-1,2-benzisoxazol-3(2H)-one derivative represented by general formula wherein R5 is a methyl group that is substituted with one or more optionally substituted phenyl groups, or an opti