1449478-01-6

Basic information

• Product Name: 3-(4-methoxybenzyl)-2-(4-fluorophenyl)-2,3-dihydrobenzo[d][1,3,2]diazaborinin-4(1H)-one
• CAS NO: 1449478-01-6
• Molecular Weight: 360.196
• Mol File: 1449478-01-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-(4-methoxybenzyl)-2-(4-fluorophenyl)-2,3-dihydrobenzo[d][1,3,2]diazaborinin-4(1H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-methoxybenzyl)-2-(4-fluorophenyl)-2,3-dihydrobenzo[d][1,3,2]diazaborinin-4(1H)-one(1449478-01-6)
• EPA Substance Registry System: 3-(4-methoxybenzyl)-2-(4-fluorophenyl)-2,3-dihydrobenzo[d][1,3,2]diazaborinin-4(1H)-one(1449478-01-6)

Safety Data

• Hazardous Substances Data: 1449478-01-6(Hazardous Substances Data)

Upstream product

• 2393-23-9 4-methoxy-benzylamine 
• 1765-93-1 4-fluoroboronic acid 
• 221539-30-6 2-amino-N-(4-methoxybenzyl)benzamide 
• 118-48-9 isatoic anhydride 

Relevant articles and documents

Green synthesis of new boron-containing quinazolines: Preparation of benzo[d][1,3,2]diazaborinin-4(1H)-one derivatives

A series of new boron-containing quinazolinones, benzo[d][1,3,2] diazaborinin-4(1H)-one derivatives, were synthesized by the sequential one-pot reaction of isatoic anhydride, amines, and arylboronic acids in the absence of a catalyst and solvent. Heating isotoic anhydride and amines led to the formation of 2-aminobenzamide intermediates, which reacted easily with boronic acids to obtain the title compounds in good yields. Solvent-free conditions provided a unique procedure because the corresponding products were not obtained using various solvents either under reflux conditions or at room temperature.