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CAS 1706447-06-4

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5-Chloro-2-methyl-4-(trifluoromethoxy)benzenesulfonyl chloride

Description:
5-Chloro-2-methyl-4-(trifluoromethoxy)benzenesulfonyl chloride is a chemical compound characterized by its sulfonyl chloride functional group, which is known for its reactivity and utility in organic synthesis. This compound features a chlorinated aromatic ring, which contributes to its electrophilic properties, making it a valuable intermediate in the synthesis of various pharmaceuticals and agrochemicals. The presence of the trifluoromethoxy group enhances its lipophilicity and may influence its biological activity. Additionally, the sulfonyl chloride moiety is highly reactive, allowing for the introduction of various nucleophiles in substitution reactions. This compound is typically handled with care due to its potential to release toxic gases upon hydrolysis and its corrosive nature. Its applications may include use in the development of sulfonamide derivatives and other complex organic molecules. As with many sulfonyl chlorides, it is important to consider its stability under different conditions and its compatibility with various solvents and reagents during chemical reactions.
Formula:C8H5Cl2F3O3S
InChI:InChI=1S/C8H5Cl2F3O3S/c1-4-2-6(16-8(11,12)13)5(9)3-7(4)17(10,14)15/h2-3H,1H3
InChI key:InChIKey=DGJYYWCBRHWJEO-UHFFFAOYSA-N
SMILES:O(C(F)(F)F)C1=C(Cl)C=C(S(Cl)(=O)=O)C(C)=C1
Synonyms:
  • Benzenesulfonyl chloride, 5-chloro-2-methyl-4-(trifluoromethoxy)-
  • 5-Chloro-2-methyl-4-(trifluoromethoxy)benzenesulfonyl chloride
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