186023
4-Chloro-7-(trifluoromethyl)quinoline
98%
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About This Item
Empirical Formula (Hill Notation):
C10H5ClF3N
CAS Number:
Molecular Weight:
231.60
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
206-471-0
MDL number:
Product Name
4-Chloro-7-(trifluoromethyl)quinoline, 98%
InChI key
LLRQVSZVVAKRJA-UHFFFAOYSA-N
InChI
1S/C10H5ClF3N/c11-8-3-4-15-9-5-6(10(12,13)14)1-2-7(8)9/h1-5H
SMILES string
FC(F)(F)c1ccc2c(Cl)ccnc2c1
assay
98%
mp
69-71 °C (lit.)
solubility
chloroform: soluble 25 mg/mL, clear, colorless
functional group
chloro
fluoro
Application
4-Chloro-7-(trifluoromethyl)quinolone was used in the synthesis of (4-substituted phenyl-1-piperazinyl) alkyl 2-aminobenzoates and 2-aminonicotinates.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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P M Manoury et al.
Journal of medicinal chemistry, 22(5), 554-559 (1979-05-01)
A series of (4-substituted phenyl-1-piperazinyl)alkyl 2-aminobenzoates and 2-aminonicotinates has been prepared and screened for analgesic and antiinflammatory properties in mice and rats. The tabulated results reveal several 2-(4-substituted phenyl-1-piperazinyl)ethyl 2-(7- or 8-substituted 4-quinolinylamino)benzoates to be six to nine times more
Mostafa M Ghorab et al.
Acta pharmaceutica (Zagreb, Croatia), 64(3), 285-297 (2014-10-10)
Novel nineteen compounds based on a 4-aminoquinoline scaffold were designed and synthesized as potential antiproliferative agents. The new compounds were N-substituted at the 4-position by aryl or heteroaryl (1-9), quinolin- 3-yl (10), 2-methylquinolin-3-yl (11), thiazol-2-yl (12), and dapsone moieties (13
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