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CAS 889944-76-7

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6-Chloro-4-methyl-3-pyridinesulfonyl chloride

Description:
6-Chloro-4-methyl-3-pyridinesulfonyl chloride is an organic compound characterized by its pyridine ring structure, which is substituted with a chlorine atom and a sulfonyl chloride group. This compound typically appears as a solid or liquid, depending on the specific conditions, and is known for its reactivity due to the presence of the sulfonyl chloride functional group, which can participate in nucleophilic substitution reactions. The chlorine atom at the 6-position and the methyl group at the 4-position of the pyridine ring contribute to its unique chemical properties, influencing its solubility and reactivity. It is often used in organic synthesis, particularly in the preparation of sulfonamide derivatives and other pharmaceuticals. Safety precautions are necessary when handling this compound, as sulfonyl chlorides can be corrosive and may release toxic gases upon reaction with water or moisture. Overall, 6-Chloro-4-methyl-3-pyridinesulfonyl chloride is a valuable intermediate in chemical synthesis, particularly in medicinal chemistry.
Formula:C6H5Cl2NO2S
InChI:InChI=1S/C6H5Cl2NO2S/c1-4-2-6(7)9-3-5(4)12(8,10)11/h2-3H,1H3
InChI key:InChIKey=BYILBFFYTJJANW-UHFFFAOYSA-N
SMILES:S(Cl)(=O)(=O)C=1C(C)=CC(Cl)=NC1
Synonyms:
  • 6-Chloro-4-methyl-3-pyridinesulfonyl chloride
  • 3-Pyridinesulfonyl chloride, 6-chloro-4-methyl-
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