174759-01-4

Basic information

• Product Name: 6-bromo-2-phenyl-3-amino-4(3H)-quinazolinone
• CAS NO: 174759-01-4
• Molecular Weight: 478.299
• Mol File: 174759-01-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 6-bromo-2-phenyl-3-amino-4(3H)-quinazolinone(CAS DataBase Reference)
• NIST Chemistry Reference: 6-bromo-2-phenyl-3-amino-4(3H)-quinazolinone(174759-01-4)
• EPA Substance Registry System: 6-bromo-2-phenyl-3-amino-4(3H)-quinazolinone(174759-01-4)

Safety Data

• Hazardous Substances Data: 174759-01-4(Hazardous Substances Data)

Upstream product

• 2280-44-6 D-Glucose 
• 115754-65-9 6-bromo-2-phenyl-3-amino-4(3H)-quinazolinone 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 160008-43-5 6-bromo-2-phenyl-3-amino-4(3H)-quinazolinone 

Downstream Products

• 170299-18-0 6-bromo-2-phenyl-3-amino-4(3H)-quinazolinone 

Relevant articles and documents

Reaction of 6-Substituted 3-Amino-2-aryl-4(3H)-quinazolinones with D-Glucose and D-Galactose

The reaction of 6-substituted 3-amino-2-aryl-4(3H)-quinazolinones (1-5) with D-Glucose and D-Galactose in boiling methanol in the presence of acetic acid as a catalyst yielded a mixture of α- and β-anomers of 6-substituted 2-aryl-3--amino-4-(3H)-quinazolinones.The N-glycopyranoside derivatives 6-12 were acetylated with acetic anhydride/pyridine to give the corresponding acetates 13-19.Deacetylation of 13, 14, 18, 19 gave 6-substituted 2-aryl-3--amino-4(3H)-quinazolinones (20-23) as sterically hindered exo- andendo-isomers.Key words: N-glycopyranoside, cerbohydicles