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CAS 68631-04-9

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2,3-Dimethyl-5-nitrobenzenesulfonyl chloride

Description:
2,3-Dimethyl-5-nitrobenzenesulfonyl chloride is an organic compound characterized by its sulfonyl chloride functional group, which is known for its reactivity in various chemical reactions, particularly in the formation of sulfonamides. This compound features a benzene ring substituted with two methyl groups at the 2 and 3 positions, and a nitro group at the 5 position, contributing to its unique chemical properties. The presence of the sulfonyl chloride group makes it a potent electrophile, allowing it to participate in nucleophilic substitution reactions. It is typically used in organic synthesis, particularly in the preparation of sulfonamides and other derivatives. The compound is generally handled with care due to its potential to release toxic gases upon hydrolysis and its corrosive nature. In terms of physical properties, it is usually a solid at room temperature, with a specific melting point and solubility characteristics that depend on the solvent used. Proper safety measures should be taken when working with this compound, including the use of personal protective equipment.
Formula:C8H8ClNO4S
InChI:InChI=1S/C8H8ClNO4S/c1-5-3-7(10(11)12)4-8(6(5)2)15(9,13)14/h3-4H,1-2H3
InChI key:InChIKey=VPPPQFAKKFQYGQ-UHFFFAOYSA-N
SMILES:S(Cl)(=O)(=O)C1=CC(N(=O)=O)=CC(C)=C1C
Synonyms:
  • 2,3-Dimethyl-5-nitrobenzenesulphonyl chloride
  • Benzenesulfonyl chloride, 2,3-dimethyl-5-nitro-
  • 2,3-Dimethyl-5-nitrobenzene-1-sulfonyl chloride
  • 2,3-Dimethyl-5-nitrobenzenesulfonyl chloride
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