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CAS 959996-58-8

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6-(Trifluoromethyl)-3-pyridinesulfonyl chloride

Description:
6-(Trifluoromethyl)-3-pyridinesulfonyl chloride is a chemical compound characterized by its pyridine ring, which is substituted at the 3-position with a sulfonyl chloride group and at the 6-position with a trifluoromethyl group. This compound is typically a solid at room temperature and is known for its reactivity due to the presence of the sulfonyl chloride functional group, which can participate in nucleophilic substitution reactions. The trifluoromethyl group enhances the compound's lipophilicity and can influence its biological activity, making it of interest in medicinal chemistry and agrochemical applications. The presence of fluorine atoms often imparts unique electronic properties, potentially affecting the compound's stability and reactivity. Additionally, this substance may be handled with caution due to its potential toxicity and corrosive nature, particularly in the presence of moisture, which can lead to the release of hydrochloric acid. Proper safety protocols should be followed when working with this compound in a laboratory setting.
Formula:C6H3ClF3NO2S
InChI:InChI=1S/C6H3ClF3NO2S/c7-14(12,13)4-1-2-5(11-3-4)6(8,9)10/h1-3H
InChI key:InChIKey=NSGLNIQAWVNZFB-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=CC=C(S(Cl)(=O)=O)C=N1
Synonyms:
  • 3-Pyridinesulfonyl Chloride, 6-(Trifluoromethyl)-
  • 6-(Trifluoromethyl)-3-pyridinesulfonyl chloride
  • 2-(Trifluoromethyl)pyridine-5-sulfonyl chloride
  • 6-(Trifluoromethyl)pyridine-3-sulfonyl chloride
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