556157
2-Cyanobenzenesulfonyl chloride
98%
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About This Item
Linear Formula:
NCC6H4SO2Cl
CAS Number:
Molecular Weight:
201.63
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
98%
Form:
solid
InChI
1S/C7H4ClNO2S/c8-12(10,11)7-4-2-1-3-6(7)5-9/h1-4H
SMILES string
ClS(=O)(=O)c1ccccc1C#N
InChI key
NQAYCMBZPAARNO-UHFFFAOYSA-N
assay
98%
form
solid
mp
65-69 °C (lit.)
Application
2-Cyanobenzenesulfonyl chloride may be used in the synthesis of:
- 2-butyl-5-(2-cyanophenyl)furan
- 2-(2-cyanophenyl)-3,6-dimethyl-4,5,6,7-tetrahydrobenzofuran
- 5-thia-4b,10-diaza-indeno[2,1-a]indene-5,5-dioxide
- 1-methyl-2-(2-cyanophenyl)pyrrole
signalword
Danger
hcodes
Hazard Classifications
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
Regulatory Information
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Microwave-Assisted, One-Pot Synthesis of 5-Thia-4 b, 10-diaza-indeno [2, 1-a]-indene-5, 5-dioxide and 10 H-11-Thia-5, 10 a-diaza-benzo [b] fluorene-11, 11-dioxide.
Cole AG, et al.
Synthetic Communications, 39(20), 3607-3610 (2009)
Palladium-Catalysed Direct Desulfitative Arylation of Pyrroles using Benzenesulfonyl Chlorides as Alternative Coupling Partners.
Jin R, et al.
Advanced Synthesis & Catalysis, 356(18), 3831-3841 (2014)
Benzenesulfonyl Chlorides: Alternative Coupling Partners for Regiocontrolled Palladium-Catalyzed Direct Desulfitative 5-Arylation of Furans.
Beladhria A, et al.
Synthesis, 46(18), 2515-2523 (2014)
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