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186023

Sigma-Aldrich

4-Chloro-7-(trifluoromethyl)quinoline

98%

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About This Item

Empirical Formula (Hill Notation):
C10H5ClF3N
CAS Number:
346-55-4
Molecular Weight:
231.60
EC Number:
206-471-0
MDL number:
MFCD00006775
UNSPSC Code:
12352100
PubChem Substance ID:
24851198
NACRES:
NA.22

assay

98%

mp

69-71 °C (lit.)

solubility

chloroform: soluble 25 mg/mL, clear, colorless

SMILES string

FC(F)(F)c1ccc2c(Cl)ccnc2c1

InChI

1S/C10H5ClF3N/c11-8-3-4-15-9-5-6(10(12,13)14)1-2-7(8)9/h1-5H

InChI key

LLRQVSZVVAKRJA-UHFFFAOYSA-N

Application

4-Chloro-7-(trifluoromethyl)quinolone was used in the synthesis of (4-substituted phenyl-1-piperazinyl) alkyl 2-aminobenzoates and 2-aminonicotinates.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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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