67571-01-1

Basic information

• Product Name: 1H-Pyridazino[6,1-b]quinazoline-2,10-dione, 3,4,4a,5-tetrahydro-4a-methyl-1-phenyl-
• CAS NO: 67571-01-1
• Molecular Formula: C18H17N3O2
• Molecular Weight: 307.352
• Mol File: 67571-01-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1H-Pyridazino[6,1-b]quinazoline-2,10-dione, 3,4,4a,5-tetrahydro-4a-methyl-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyridazino[6,1-b]quinazoline-2,10-dione, 3,4,4a,5-tetrahydro-4a-methyl-1-phenyl-(67571-01-1)
• EPA Substance Registry System: 1H-Pyridazino[6,1-b]quinazoline-2,10-dione, 3,4,4a,5-tetrahydro-4a-methyl-1-phenyl-(67571-01-1)

Safety Data

• Hazardous Substances Data: 67571-01-1(Hazardous Substances Data)

Upstream product

• 123-76-2 levulinic acid 
• 30086-49-8 2-amino-N'-phenylbenzohydrazide 
• 100-63-0 phenylhydrazine 
• 118-92-3 anthranilic acid 

Relevant articles and documents

A diversity oriented synthesis of 2,10-dioxo-10H-1,2,3,4,4a,5-hexahydropyridazino[3,2-b]quinazolines

A parallel method for the synthesis of the title compounds is described. Thus, methyl anthranilates (5) are transformed into 2-aminobenzohydrazides (3) which were treated with 4-oxo acids (4) to afford in high yields and acceptable purity of piridazino[3,2-b]quinazolines (1). Compounds (1) present four diversity centers (R1, R2, R3, and R4). The range of chemically acceptable substituents at each center has been evaluated. The isolation of a possible intermediate in the formation of 1, which presents an amino structure (10), has allowed proposing a complete mechanistic rationalization for the formation of structures (1).