84571-10-8

Basic information

• Product Name: Quinazoline, 1,2,3,4-tetrahydro-2-(3-nitrophenyl)-
• CAS NO: 84571-10-8
• Molecular Formula: C14H13N3O2
• Molecular Weight: 255.276
• Mol File: 84571-10-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Quinazoline, 1,2,3,4-tetrahydro-2-(3-nitrophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Quinazoline, 1,2,3,4-tetrahydro-2-(3-nitrophenyl)-(84571-10-8)
• EPA Substance Registry System: Quinazoline, 1,2,3,4-tetrahydro-2-(3-nitrophenyl)-(84571-10-8)

Safety Data

• Hazardous Substances Data: 84571-10-8(Hazardous Substances Data)

Upstream product

• 99-61-6 3-nitro-benzaldehyde 
• 1885-29-6 anthranilic acid nitrile 
• 140429-24-9 N-[chloro(3-nitrophenyl)methyl]pyridinium chloride 
• 4403-69-4 2-amino-1-benzylamine 

Relevant articles and documents

Design, synthesis, and enzymatic characterization of quinazoline-based CYP1A2 inhibitors

Cytochrome P450 isozyme 1A2 (CYP1A2) is one main xenobiotic metabolizing enzyme in humans. It has been associated with the bioactivation of procarcinogens, including 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK), a tobacco specific and potent pulmo

A convenient one-pot procedure for the synthesis of 2-aryl quinazolines using active MnO2 as oxidant

(Chemical Equation Presented) A variety of 2-aryl quinazolines were synthesized from the condensation of 2-aminobenzylamines and aryl aldehydes to form 2-aryl-1,2,3,4-tetrahydroquinazolines and subsequent oxidation of the intermediates with MnO2/sub

Synthesis of 3,1-benzoxazines and tetrahydroquinazolines from o-aminobenzyl alcohol and o-aminobenzyl amine - Semi-empirical MO calculations

o-Aminobenzyl alcohol (4) reacts with aldehydes and ketones to the 3,1-benzoxazines 20a/b and 22a/b, whereas the enamine derivatives 24a-c are formed from β-diketones. The isosteric o-amino-benzylamine (1) gives tetrahydroquinazolines 11a/b and 14b as het