158836
2-甲基-4(3H)-喹唑啉酮
97%
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关于此项目
经验公式（希尔记法）:
C9H8N2O
化学文摘社编号:
分子量:
160.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
217-189-2
MDL number:
Assay:
97%
Form:
powder
InChI key
FIEYHAAMDAPVCH-UHFFFAOYSA-N
InChI
1S/C9H8N2O/c1-6-10-8-5-3-2-4-7(8)9(12)11-6/h2-5H,1H3,(H,10,11,12)
SMILES string
CC1=Nc2ccccc2C(=O)N1
assay
97%
form
powder
mp
231-233 °C (lit.)
Application
2-Methyl-4(3H)-quinazolinone may be used in chemical synthesis.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - 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
Production of 2-methyl-4[3H]-quinazolinone, an inhibitor of poly(ADP-ribose) synthetase, by bacterium.
S Yoshida et al.
The Journal of antibiotics, 44(1), 111-112 (1991-01-01)
Kollur Shiva Prasad et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 107, 108-116 (2013-02-19)
Four novel mononuclear Pd(II) complexes have been synthesized with the biologically active Schiff base ligands (L1-L4) derived from 3-amino-2-methyl-4(3H)-quinazolinone. The structure of the complexes has been proposed by elemental analysis, molar conductance, IR, (1)H NMR, mass, UV-Vis spectrometric and thermal
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