CAS 1060811-16-6
:2-(Trifluoromethyl)-3-pyridinesulfonyl chloride
Description:
2-(Trifluoromethyl)-3-pyridinesulfonyl chloride is a chemical compound characterized by its unique functional groups and structure. It features a pyridine ring substituted with a trifluoromethyl group and a sulfonyl chloride moiety, which contributes to its reactivity and potential applications in organic synthesis. The presence of the trifluoromethyl group enhances the compound's lipophilicity and can influence its biological activity, while the sulfonyl chloride group is known for its ability to act as a versatile electrophile in nucleophilic substitution reactions. This compound is typically used in the synthesis of various pharmaceuticals and agrochemicals, owing to its ability to introduce the sulfonyl chloride functionality into target molecules. Additionally, it may exhibit properties such as high stability under certain conditions, but it can also be reactive, particularly with nucleophiles. Safety precautions are essential when handling this compound, as sulfonyl chlorides can release toxic gases upon hydrolysis. Overall, its distinctive structure and reactivity make it a valuable intermediate in chemical synthesis.
Formula:C6H3ClF3NO2S
InChI:InChI=1S/C6H3ClF3NO2S/c7-14(12,13)4-2-1-3-11-5(4)6(8,9)10/h1-3H
InChI key:InChIKey=IRINAFUPYRWEKL-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=C(S(Cl)(=O)=O)C=CC=N1
Synonyms:- 3-Pyridinesulfonyl chloride, 2-(trifluoromethyl)-
- 2-(Trifluoromethyl)-3-pyridinesulfonyl chloride
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Found 2 products.
2-(Trifluoromethyl)pyridine-3-sulfonyl chloride
CAS:Formula:C6H3ClF3NO2SPurity:95.0%Molecular weight:245.62-(Trifluoromethyl)pyridine-3-sulfonyl Chloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H3NO2F3SClPurity:Min. 95%Molecular weight:245.6 g/mol

