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Merck
CN

545708

2,6-Dichlorobenzenesulfonyl chloride

97%

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About This Item

Linear Formula:
Cl2C6H3SO2Cl
CAS Number:
Molecular Weight:
245.51
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
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Quality Level

assay

97%

mp

53-56 °C (lit.)

functional group

chloro

SMILES string

Clc1cccc(Cl)c1S(Cl)(=O)=O

InChI

1S/C6H3Cl3O2S/c7-4-2-1-3-5(8)6(4)12(9,10)11/h1-3H

InChI key

WGGKQIKICKLWGN-UHFFFAOYSA-N

General description

2,6-Dichlorobenzenesulfonyl chloride, also known as 2,6-dichlorophenylsulfonyl chloride, is an aryl sulfonyl chloride derivative.

Application

2,6-Dichlorobenzenesulfonyl chloride may be used as a starting material in the multi-step synthesis of sulfonamide-containing diarylsquaramide. It may also be used in the synthesis of cycloheptyl substituted 1,2,4-triazolopyridine (TZP) analogs.


pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

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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Brent W McCleland et al.
Bioorganic & medicinal chemistry letters, 17(6), 1713-1717 (2007-01-24)
N,N'-diarylsquaramides were prepared and evaluated as antagonists of CXCR2. The compounds were found to be potent and selective antagonists of CXCR2. Significant differences in SAR was observed relative to the previously described N,N'-diarylurea series. As was the case in the
Haixia Wang et al.
Bioorganic & medicinal chemistry letters, 21(14), 4146-4149 (2011-06-22)
A series of pyridyl amide/sulfonamide inhibitors of 11β-HSD-1 were modified to incorporate a novel 1,2,4-triazolopyridine scaffold. Optimization of substituents at the 3 and 8 position of the TZP core, with a special focus on enhancing metabolic stability, resulted in the



Global Trade Item Number

SKUGTIN
545708-5G04061832419633
545708-1G04061825896465