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关于此项目
经验公式(希尔记法):
C10H8Cl2N2O2
化学文摘社编号:
分子量:
259.09
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
产品名称
2,4-二氯-6,7-二甲氧基喹唑啉, 97%
InChI
1S/C10H8Cl2N2O2/c1-15-7-3-5-6(4-8(7)16-2)13-10(12)14-9(5)11/h3-4H,1-2H3
SMILES string
COc1cc2nc(Cl)nc(Cl)c2cc1OC
InChI key
DGHKCBSVAZXEPP-UHFFFAOYSA-N
assay
97%
mp
175-178 °C (lit.)
functional group
chloro
Quality Level
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Application
2,4-Dichloro-6,7-dimethoxyquinazoline may be used as a reactant in the preparation of the following potential bioactive compounds:
- 2-chloro-4,6,7-trimethoxyquinazoline
- 2-chloro-6,7-dimethoxy-4(3H)-quinazolinone
- 2,4-diamino-6,7-dimethoxy quinazolines
- 2-chloro-4-(3-bromoanilino)-6,7-dimethoxyquinazoline
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
Discovery of a 2, 4-diamino-7-aminoalkoxyquinazoline as a potent and selective inhibitor of histone lysine methyltransferase G9a.
Liu F, et al.
Journal of Medicinal Chemistry, 52(24), 7950-7953 (2009)
A short and unequivocal synthesis of 5-aminotetrazolo[1,5-a]-quinazoline as a tricyclic analogue of 4-(3-bromoanilino)-6,7-dimethoxyquinazoline (PD 153035).
Bencteux E and Houssin R.
Journal of Heterocyclic Chemistry, 34(4), 1375-1378 (1997)
Antihypertensive 2-amino-4 (3H)-quinazolinones.
Hess HJ, et al.
Journal of Medicinal Chemistry, 11(1), 130-136 (1968)
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