InChI
1S/C9H9N3O/c1-6-11-8-5-3-2-4-7(8)9(13)12(6)10/h2-5H,10H2,1H3
SMILES string
CC1=Nc2ccccc2C(=O)N1N
InChI key
IQOUPYQSZBDNAW-UHFFFAOYSA-N
assay
98%
form
solid
mp
149-152 °C (lit.)
General description
3-Amino-2-methyl-4(3H)quinazolinone is a quinazoline derivative. 2-Methyl-3,1-benzoxazin-4-one undergoes condensation reaction with hydrazine hydrate to yield 3-amino-2-methyl-4(3H)quinazolinone. It undergoes condensation with various substituted aldehydes to afford Schiff′s bases.
Application
3-Amino-2-methyl-4(3H)quinazolinone may be used to synthesize:
- 2-methyl-3-[3′-aminophthalimido]-4(3H)-quinazolinone
- 2-alkyl-3-(methylamino)-4(3H)-quinazolinone
- 3-amino-2-chloromethyl-4(3H)-quinazolinone
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Disperse dyes based on 2-methyl-3-[3'-amino-phthalimido]-4 (3H)-quinazilinone.
Patel VH, et al.
J. Serb. Chem. Soc., 67(11), 719-726 (2002)
Dipolar Cycloaddition Reactions with Quinazolinones: A New Route for the Synthesis of Several Annelated Pyrrolo-and Pyridazinoquinazoline Derivatives.
Ghabrial SS and Gaber HM.
Molecules (Basel), 8(5), 401-410 (2003)
Lithiation of 2-Alkyl-3-amino-and 2-Alkyl-3-(methylamino)-4 (3 H)-quinazolinones1.
Smith K, et al.
The Journal of Organic Chemistry, 61(2), 656-661 (1996)
Kollur Shiva Prasad et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 81(1), 276-282 (2011-07-12)
Four Schiff base ligands and their corresponding organotin(IV) complexes have been synthesized and characterized by elemental analyses, IR, (1)H NMR, MS and thermal studies. The Schiff bases are obtained by the condensation of 3-amino-2-methyl-4(3H)-quinazolinone with different substituted aldehydes. The elemental
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