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Assay
98%
form
solid
mp
65-69 °C (lit.)
SMILES string
ClS(=O)(=O)c1ccccc1C#N
InChI
1S/C7H4ClNO2S/c8-12(10,11)7-4-2-1-3-6(7)5-9/h1-4H
InChI key
NQAYCMBZPAARNO-UHFFFAOYSA-N
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
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Find documentation for the products that you have recently purchased in the Document Library.
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.
Synthetic Communications, 39(20), 3607-3610 (2009)
Palladium-Catalysed Direct Desulfitative Arylation of Pyrroles using Benzenesulfonyl Chlorides as Alternative Coupling Partners.
Advanced Synthesis & Catalysis, 356(18), 3831-3841 (2014)
Benzenesulfonyl Chlorides: Alternative Coupling Partners for Regiocontrolled Palladium-Catalyzed Direct Desulfitative 5-Arylation of Furans.
Synthesis, 46(18), 2515-2523 (2014)
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