1597437-68-7

Basic information

• Product Name: 3-(2-aminoethyl)-2-[3-methylanilino]quinazolin-4(3H)-one
• Synonyms: 3-(2-aminoethyl)-2-[3-methylanilino]quinazolin-4(3H)-one
• CAS NO: 1597437-68-7
• Molecular Weight: 294.356
• Mol File: 1597437-68-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-(2-aminoethyl)-2-[3-methylanilino]quinazolin-4(3H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2-aminoethyl)-2-[3-methylanilino]quinazolin-4(3H)-one(1597437-68-7)
• EPA Substance Registry System: 3-(2-aminoethyl)-2-[3-methylanilino]quinazolin-4(3H)-one(1597437-68-7)

Safety Data

• Hazardous Substances Data: 1597437-68-7(Hazardous Substances Data)

Upstream product

• 118-92-3 anthranilic acid 
• 31162-13-7 2-azidobenzoic acid 
• 90408-05-2 o-azidobenzoic acid ethyl ester 
• 179039-70-4 ethyl 2-(triphenylphosphoranylidene-amino)benzoate 
• 621-30-7 3-methylphenyl isothiocyanate 
• 107-15-3 ethylenediamine 

Downstream Products

• 1597437-86-9 (E)-3-[2-((2,6-dichlorobenzylidene)amino)ethyl]-2-(3-methylanilino)quinazolin-4(3H)-one 
• 1597437-84-7 (E)-3-[2-((4-(dimethylamino)benzylidene)amino)ethyl]-2-(3-methylanilino)quinazolin-4(3H)-one 
• 1597437-87-0 (E)-3-[2-((4-fluorobenzylidene)amino)ethyl]-2-(3-methylanilino)quinazolin-4(3H)-one 
• 1597437-88-1 (E)-3-[2-((4-hydroxybenzylidene)amino)ethyl]-2-(3-methylanilino)quinazolin-4(3H)-one 

Relevant articles and documents

Design, synthesis, and evaluation of new 4(3H)-quinazolinone derivatives containing a pyrazole carboxamide moiety

A total of 15 new 4(3H)-quinazolinone derivatives containing a pyrazole carboxamide moiety were designed and synthesized in this study. The structures of the target compounds were elucidated using 1H NMR, 13C NMR, MS, and elemental a

Design, synthesis, and antibacterial activity of novel Schiff base derivatives of quinazolin-4(3H)-one

Novel imine derivatives of quinazolin-4(3H)-one were designed and synthesized by using aminoethyl moieties to increase the amine bridge of quinazolin-4(3H)-one amine and then introducing various aromatic aldehydes. The target compounds were characterized