CAS 1242339-40-7
:5-Chloro-4-fluoro-2-methylbenzenesulfonyl chloride
Description:
5-Chloro-4-fluoro-2-methylbenzenesulfonyl chloride is an organic compound characterized by the presence of a sulfonyl chloride functional group attached to a substituted aromatic ring. The compound features a chlorinated and fluorinated benzene ring, which contributes to its reactivity and potential applications in organic synthesis. The sulfonyl chloride group is known for its ability to act as a sulfonating agent, making this compound useful in the preparation of sulfonamides and other derivatives. It is typically a colorless to pale yellow liquid or solid, depending on its form and purity. The presence of chlorine and fluorine atoms enhances its electrophilic character, allowing it to participate in various nucleophilic substitution reactions. Due to its reactive nature, appropriate safety precautions should be taken when handling this compound, as it can be corrosive and may pose health hazards. Its applications may extend to pharmaceuticals, agrochemicals, and materials science, where it can serve as an intermediate in the synthesis of more complex molecules.
Formula:C7H5Cl2FO2S
InChI:InChI=1S/C7H5Cl2FO2S/c1-4-2-6(10)5(8)3-7(4)13(9,11)12/h2-3H,1H3
InChI key:InChIKey=RAYLWLGLEWDHBZ-UHFFFAOYSA-N
SMILES:S(Cl)(=O)(=O)C1=C(C)C=C(F)C(Cl)=C1
Synonyms:- 5-Chloro-4-fluoro-2-methylbenzenesulfonyl chloride
- Benzenesulfonyl chloride, 5-chloro-4-fluoro-2-methyl-
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Found 3 products.
5-Chloro-4-fluoro-2-methylbenzenesulfonyl chloride
CAS:Formula:C7H5Cl2FO2SPurity:98%Molecular weight:243.08285-Chloro-4-fluoro-2-methylbenzenesulfonyl chloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H5Cl2FO2SPurity:Min. 95%Molecular weight:243.09 g/mol


