CAS 1744-43-0
:2-FLUORO-5-(TRIFLUOROMETHYL)BENZENESULPHONYL CHLORIDE
Description:
2-Fluoro-5-(trifluoromethyl)benzenesulphonyl chloride, with the CAS number 1744-43-0, is a chemical compound characterized by its sulphonyl chloride functional group, which is known for its reactivity in various organic synthesis reactions. This compound features a fluorinated aromatic ring, specifically with a fluoro group and a trifluoromethyl group, which contribute to its unique electronic properties and influence its reactivity. The presence of the sulphonyl chloride group makes it a potent electrophile, allowing it to participate in nucleophilic substitution reactions, often used in the synthesis of sulphonamides and other derivatives. It is typically a colorless to pale yellow liquid or solid, depending on the temperature and purity, and is sensitive to moisture, requiring careful handling and storage. Due to its reactivity, it is important to use appropriate safety measures when working with this compound, as it can release toxic gases upon hydrolysis. Overall, its unique structure and reactivity make it valuable in the field of organic chemistry and pharmaceuticals.
Formula:C7H3ClF4O2S
Synonyms:- 2-Fluoro-5-(Trifluoromethyl)Benzenesulfonyl Chloride
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Found 3 products.
2-Fluoro-5-(trifluoromethyl)benzene-1-sulfonyl chloride
CAS:Formula:C7H3ClF4O2SPurity:98%Color and Shape:LiquidMolecular weight:262.60912-Fluoro-5-(trifluoromethyl)benzenesulphonyl chloride
CAS:2-Fluoro-5-(trifluoromethyl)benzenesulphonyl chlorideFormula:C7H3ClF4O2SPurity:98%Color and Shape: clear. colourless liquidMolecular weight:262.61g/mol2-Fluoro-5-trifluoromethylbenzenesulfonyl chloride
CAS:Formula:C7H3ClF4O2SPurity:98%Color and Shape:Liquid, ClearMolecular weight:262.6


