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CAS 116827-38-4

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2-(Trifluoromethoxy)benzylsulphonyl chloride

Description:
2-(Trifluoromethoxy)benzylsulphonyl chloride is a chemical compound characterized by its sulphonyl chloride functional group, which is known for its reactivity in various organic synthesis applications. The presence of the trifluoromethoxy group enhances its electrophilic properties, making it a useful intermediate in the synthesis of pharmaceuticals and agrochemicals. This compound typically appears as a colorless to pale yellow liquid or solid, depending on the specific conditions. It is soluble in organic solvents but may be less soluble in water due to its hydrophobic characteristics. The sulphonyl chloride moiety is particularly reactive, allowing for nucleophilic substitution reactions with amines, alcohols, and other nucleophiles. Safety precautions are necessary when handling this compound, as it can be corrosive and may release toxic gases upon reaction with water or moisture. Overall, 2-(Trifluoromethoxy)benzylsulphonyl chloride is valued in synthetic chemistry for its versatility and reactivity.
Formula:C8H6ClF3O3S
InChI:InChI=1/C8H6ClF3O3S/c9-16(13,14)5-6-3-1-2-4-7(6)15-8(10,11)12/h1-4H,5H2
SMILES:c1ccc(c(c1)CS(=O)(=O)Cl)OC(F)(F)F
Synonyms:
  • 1-(Chlormethyl)-2-(trifluormethoxy)benzol
  • 1-(Chloromethyl)-2-(trifluoromethoxy)benzene
  • 2-(Chloromethyl)phenyl trifluoromethyl ether
  • Benzene, 1-(Chloromethyl)-2-(Trifluoromethoxy)-
  • [2-(Trifluoromethoxy)Phenyl]Methanesulfonyl Chloride
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