130532
5,7-二氯-8-羟基-2-甲基喹啉
98%
别名:
5,7-二氯-2-甲基-8-羟基喹啉, 5,7-二氯-8-羟基喹哪啶, BCM, 氯喹那多
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经验公式（希尔记法）:
C10H7Cl2NO
化学文摘社编号:
分子量:
228.07
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-789-3
Beilstein/REAXYS Number:
156683
MDL number:
Assay:
98%
assay
98%
InChI key
GPTXWRGISTZRIO-UHFFFAOYSA-N
InChI
1S/C10H7Cl2NO/c1-5-2-3-6-7(11)4-8(12)10(14)9(6)13-5/h2-4,14H,1H3
SMILES string
Cc1ccc2c(Cl)cc(Cl)c(O)c2n1
mp
108-112 °C (dec.) (lit.)
functional group
chloro
Quality Level
signalword
Warning
hcodes
pcodes
Hazard Classifications
Acute Tox. 4 Oral
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
Polymorphism and color dimorphism of chlorquinaldol (5,7-dichloro-8-hydroxy-2-methylquinoline).
A V Pavlova et al.
Die Pharmazie, 40(10), 730-730 (1985-10-01)
[Therapeutic trial of the combination promestriene-chlorquinaldol in the treatment of vaginitis].
J Senèze et al.
Revue francaise de gynecologie et d'obstetrique, 80(5), 323-325 (1985-04-01)
[Diflucortolone valerate and chlorquinaldol in topical eczema (in single or combination form)].
C Solaroli et al.
Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia, 122(5), XXXI-XXXIII (1987-05-01)
A Neiger et al.
Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis, 79(31-32), 918-920 (1990-08-02)
Besides the various operative procedures, which nowadays have come into use in hemorrhoidal disorders, drug therapy as well continues to keep an important place. Its main conditions of application are inflammatory processes before, between and after hemorrhoidal sclerosis or proctological
Tzu-Shean Feng et al.
Biochemical pharmacology, 82(3), 236-247 (2011-05-21)
4-Aminoquinolines were hybridized with artemisinin and 1,4-naphthoquinone derivatives via the Ugi-four-component condensation reaction, and their biological activities investigated. The artemisinin-containing compounds 6a-c and its salt 6c-citrate were the most active target compounds in the antiplasmodial assays. However, despite the potent
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