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Q1506

Sigma-Aldrich

8-Quinolinesulfonyl chloride

98%

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About This Item

Empirical Formula (Hill Notation):
C9H6ClNO2S
CAS Number:
18704-37-5
Molecular Weight:
227.67
Beilstein/REAXYS Number:
156347
EC Number:
242-515-5
MDL number:
MFCD00006808
UNSPSC Code:
12352100
PubChem Substance ID:
24899204
NACRES:
NA.22

Quality Level

300

assay

98%

mp

126-129 °C (lit.)

SMILES string

ClS(=O)(=O)c1cccc2cccnc12

InChI

1S/C9H6ClNO2S/c10-14(12,13)8-5-1-3-7-4-2-6-11-9(7)8/h1-6H

InChI key

JUYUYCIJACTHMK-UHFFFAOYSA-N

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pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Vijay K Agrawal et al.
European journal of medicinal chemistry, 39(7), 593-600 (2004-07-09)
Quantitative structure-activity-relationship (QSAR) study on aromatic/heterocyclic sulfonamides containing 8-quinoline-sulfonyl carbonic anhydrase (CA) inhibitors has been carried out topologically using first-order valence connectivity index ((1)chi(v)). Excellent results are obtained against all the three isozymes; CA I, II and IV of the
J Borras et al.
Bioorganic & medicinal chemistry, 7(11), 2397-2406 (2000-01-13)
Reaction of 20 aromatic/heterocyclic sulfonamides containing a free amino, imino, hydrazino or hydroxyl group, with 8-quinoline-sulfonyl chloride afforded a series of water-soluble (as hydrochloride or triflate salts) compounds. The new derivatives were assayed as inhibitors of the zinc enzyme carbonic

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