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CAS 102153-63-9

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6-Chloronaphthalene-2-sulfonyl chloride

Description:
6-Chloronaphthalene-2-sulfonyl chloride is an organic compound characterized by its sulfonyl chloride functional group attached to a chlorinated naphthalene ring. This compound typically appears as a solid, often white to light yellow in color, and is known for its reactivity due to the presence of the sulfonyl chloride group, which can undergo nucleophilic substitution reactions. It is soluble in organic solvents such as dichloromethane and chloroform but is generally insoluble in water. The compound is utilized in organic synthesis, particularly in the preparation of sulfonamide derivatives and as an intermediate in the production of pharmaceuticals and agrochemicals. Due to its chlorinated structure, it may exhibit biological activity and can be subject to environmental considerations regarding its stability and degradation. Safety precautions are necessary when handling this compound, as it can be corrosive and may cause irritation to the skin, eyes, and respiratory system. Proper storage in a cool, dry place away from moisture is recommended to maintain its stability.
Formula:C10H6Cl2O2S
InChI:InChI=1S/C10H6Cl2O2S/c11-9-3-1-8-6-10(15(12,13)14)4-2-7(8)5-9/h1-6H
InChI key:InChIKey=IYFIYGSJZIICOZ-UHFFFAOYSA-N
SMILES:S(Cl)(=O)(=O)C1=CC2=C(C=C1)C=C(Cl)C=C2
Synonyms:
  • 2-Naphthalenesulfonyl chloride, 6-chloro-
  • 6-Chloro-2-naphthalenesulfonyl chloride
  • 6-Chloro-2-naphthylsulfonyl chloride
  • 6-Cloro-2-Naphthylsulfonyl Chloride
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