CymitQuimica logo

CAS 39234-86-1

:

3,5-Bis(trifluoromethyl)benzenesulfonyl chloride

Description:
3,5-Bis(trifluoromethyl)benzenesulfonyl chloride is a sulfonyl chloride compound characterized by the presence of two trifluoromethyl groups attached to a benzene ring, along with a sulfonyl chloride functional group. This compound is typically a colorless to pale yellow liquid or solid, depending on its form and purity. It is known for its high reactivity, particularly due to the sulfonyl chloride group, which can readily participate in nucleophilic substitution reactions. The trifluoromethyl groups contribute to its lipophilicity and can enhance the compound's stability and resistance to hydrolysis. This substance is often used in organic synthesis, particularly in the preparation of sulfonamides and other sulfonyl derivatives. Due to its chemical properties, it requires careful handling, as it can be corrosive and may pose health hazards upon exposure. Proper safety measures, including the use of personal protective equipment, are essential when working with this compound in a laboratory setting.
Formula:C8H3ClF6O2S
InChI:InChI=1S/C8H3ClF6O2S/c9-18(16,17)6-2-4(7(10,11)12)1-5(3-6)8(13,14)15/h1-3H
InChI key:InChIKey=BTRCVKADYDVSLI-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=CC(C(F)(F)F)=CC(S(Cl)(=O)=O)=C1
Synonyms:
  • 2-Chloro-1,1,3,4,4-Pentafluorobuta-1,3-Diene
  • 3,5-Bis(Trimethyl)Benzenesulfonyl Chloride
  • 3,5-Bis(trifluoromethyl)benzenesulfonyl chloride
  • 3,5-Di(trifluoromethyl)benzene-1-sulfonyl chloride
  • 3,5-Di(trifluoromethyl)benzenesulfonyl chloride
  • 3,5-Ditrifluoromethylbenzenesulfonyl chloride
  • Benzenesulfonyl chloride, 3,5-bis(trifluoromethyl)-
  • 3,5-Bis(trifluoromethyl)benzene-1-sulfonyl chloride
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 5 products.