31005-05-7

Basic information

• Product Name: 2H-1-Benzopyran-2-one, 7-(benzoyloxy)-
• CAS NO: 31005-05-7
• Molecular Formula: C16H10O4
• Molecular Weight: 266.253
• Mol File: 31005-05-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2H-1-Benzopyran-2-one, 7-(benzoyloxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-1-Benzopyran-2-one, 7-(benzoyloxy)-(31005-05-7)
• EPA Substance Registry System: 2H-1-Benzopyran-2-one, 7-(benzoyloxy)-(31005-05-7)

Safety Data

• Hazardous Substances Data: 31005-05-7(Hazardous Substances Data)

Upstream product

• 531-59-9 7-methoxycoumarin 
• 98-88-4 benzoyl chloride 
• 93-35-6 7-hydroxy-2H-chromen-2-one 

Downstream Products

• 856179-39-0 7-benzoyl-6-hydroxy-benzofuran-2-carboxylic acid 
• 859323-72-1 8-benzoyl-3-bromo-7-hydroxy-coumarin 
• 6748-68-1 8-acetyl-7-hydroxycoumarin 
• 2555-29-5 8-acetyl-7-hydroxy-4-methyl-2H-chromen-2-one 
• 90104-85-1 8-Benzoyl-7-hydroxycoumarin 
• 20312-83-8 8-Benzoyl-7-hydroxy-4-methylcoumarin 
• 93-35-6 7-hydroxy-2H-chromen-2-one 

Relevant articles and documents

Inhibitory effects and structural insights for a novel series of coumarin-based compounds that selectively target human CA IX and CA XII carbonic anhydrases

Coumarin derivatives are a peculiar class of inhibitors of the family of metalloenzymes carbonic anhydrases (CA, EC 4.2.1.1). Several coumarins display higher affinity and selectivity toward most relevant and druggable CA isoforms. By decorating the natur

Semisynthesis, ex vivo evaluation, and SAR studies of coumarin derivatives as potential antiasthmatic drugs

Asthma is a chronic inflammatory disorder that causes contraction in the smooth muscle of the airway and blocking of airflow. Reversal the contractile process is a strategy for the search of new drugs that could be used for the treatment of asthma. This work reports the semisynthesis, ex vivo relaxing evaluation and SAR studies of a series of 18 coumarins. The results pointed that the ether derivatives 1-3, 7-9 and 13-15 showed the best activity (E max = 100%), where compound 2 (42 μM) was the most potent, being 4-times more active than theophylline (positive control). The ether homologation (methyl, ethyl and propyl) in position 7 or positions 6 and 7 of coumarins lead to relaxing effect, meanwhile formation of esters generated less active compounds than ethers. The SAR analysis showed that it is necessary the presence of two small ether groups and the methyl group at position 4 (site 3) encourage biological activity through soft hydrophobic changes in the molecule, without drastically affecting the cLogP.

A simple and efficient transprotection of aryl methyl ether to aryl benzoate under microwave activation

A simple and efficient method for the transprotection of aryl methyl ether to easily cleavable arylbenzoate mediated by microwave activation has been developed. One important feature of this method is its high tolerance towards sensitive functionalities and to some extent to bulky environment.