1429426-07-2

Basic information

• Product Name: 2-(2-hydroxy-5-methylbenzoyl)-8-methyl-4H-furo[3,2-c]chromen-4-one
• Synonyms: 2-(2-hydroxy-5-methylbenzoyl)-8-methyl-4H-furo[3,2-c]chromen-4-one
• CAS NO: 1429426-07-2
• Molecular Weight: 334.328
• Mol File: 1429426-07-2.mol

Chemical Properties

• CAS DataBase Reference: 2-(2-hydroxy-5-methylbenzoyl)-8-methyl-4H-furo[3,2-c]chromen-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-hydroxy-5-methylbenzoyl)-8-methyl-4H-furo[3,2-c]chromen-4-one(1429426-07-2)
• EPA Substance Registry System: 2-(2-hydroxy-5-methylbenzoyl)-8-methyl-4H-furo[3,2-c]chromen-4-one(1429426-07-2)

Safety Data

• Hazardous Substances Data: 1429426-07-2(Hazardous Substances Data)

Upstream product

• 102653-68-9 3-bromo-6-methyl-4H-chromen-4-one 
• 120869-42-3 2-amino-6-methyl-4H-chromen-4-one 
• 50-00-0 formaldehyd 
• 13252-83-0 4-hydroxy-6-methylcoumarin 

Relevant articles and documents

Copper(ii) bromide-catalyzed intramolecular decarboxylative functionalization to form a C(sp3)-O bond for the synthesis of furo[3,2-c]coumarins

An efficient and eco-friendly copper(ii) bromide-catalyzed intramolecular decarboxylative functionalization to form a C(sp3)-O bond for the synthesis of furo[3,2-c]coumarins has been developed. In this reaction, a copper(ii) bromide-catalyzed intramolecular decarboxylative functionalization of α-carbonyl is successfully realized to generate an α-bromo carbonyl compound as a key intermediate.

DMSO and iodine mediated reaction of 4-hydroxycoumarins and aldehydes/aryl methyl ketones: Synthesis of furo[3,2-c]coumarins

A simple and efficient method for the synthesis of highly functionalized furo[3,2-c]coumarins was developed. The reaction occurred via initial formation of biscoumarins from the reaction of 4-hydroxycoumarins and aldehydes/aryl methyl ketones in the prese

Synthesis of furo[3,2-c]coumarin from the reaction of 3-halochromone and 2-aminochromone; 2-aminochromone as a masked 4-hydroxycoumarin

Synthesis of 2-(2-hydroxybenzoyl)-4H-furo[3,2-c]chromen-4-one has been accomplished by the reaction of 3-halochromone with 2-aminochromone. In this reaction, 2-aminochromone acts as a masked 4-hydroxycoumarin.