1092452-47-5

Basic information

• Product Name: N-[(4-bromophenyl)(4-hydroxy-2-oxo-2H-chromen-3-yl)methyl]acetamide
• Synonyms: N-[(4-bromophenyl)(4-hydroxy-2-oxo-2H-chromen-3-yl)methyl]acetamide
• CAS NO: 1092452-47-5
• Molecular Weight: 388.217
• Mol File: 1092452-47-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-[(4-bromophenyl)(4-hydroxy-2-oxo-2H-chromen-3-yl)methyl]acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(4-bromophenyl)(4-hydroxy-2-oxo-2H-chromen-3-yl)methyl]acetamide(1092452-47-5)
• EPA Substance Registry System: N-[(4-bromophenyl)(4-hydroxy-2-oxo-2H-chromen-3-yl)methyl]acetamide(1092452-47-5)

Safety Data

• Hazardous Substances Data: 1092452-47-5(Hazardous Substances Data)

Upstream product

• 60-35-5 acetamide 
• 1076-38-6 4-hydroxy[1]benzopyran-2-one 
• 1122-91-4 4-bromo-benzaldehyde 
• 75-05-8 acetonitrile 

Relevant articles and documents

An efficient and green protocol for the one-pot synthesis of 3-amido-alkyl-4-hydroxycoumarin derivatives by choline chloride/urea as a deep eutectic solvent

A green and highly efficient synthesis of some 3-amido-alkyl-4-hydroxycoumarin derivatives by one-pot, three-component reaction of aryl aldehydes, 4-hydroxycoumarin, or 4-hydroxy-6-methylpyran-1-one, and amides in deep eutectic solvent (DES) is reported.

Novel efficient three-component, one-pot synthesis of 3-(α- amidobenzyl)- 4-hydroxycoumarin derivatives

The three-component reaction between 4-hydroxycoumarin, aromatic aldehydes and amides catalysed by p-toluenesulfonic acid in solvent-free conditions provided a simple and efficient one-pot route for the synthesis of 3-(α- amidobenzyl)-4-hydroxycoumarin derivatives in excellent yields.

Synthesis of 3-[(acetylamino)(aryl)methyl]-4-hydroxycoumarins

One-pot, three-component reaction between aryl aldehydes, 4-hydroxycoumarin, and acetonitrile in the presence of chlorosulfonic acid affords 3-[(acetylamino)(aryl)methyl]-4-hydroxycoumarins in excellent yields.