CAS 629672-19-1
:4-Fluoro-3-methylbenzenesulfonyl chloride
Description:
4-Fluoro-3-methylbenzenesulfonyl chloride, with the CAS number 629672-19-1, is an organic compound characterized by the presence of a sulfonyl chloride functional group attached to a substituted aromatic ring. This compound features a fluorine atom and a methyl group on the benzene ring, which influence its reactivity and properties. It is typically a colorless to pale yellow liquid or solid, depending on the temperature and purity. The sulfonyl chloride group makes it a potent electrophile, allowing it to participate in various chemical reactions, such as nucleophilic substitutions, which are valuable in synthetic organic chemistry. The presence of the fluorine atom can enhance the compound's stability and alter its electronic properties, making it useful in the development of pharmaceuticals and agrochemicals. Additionally, due to the reactive nature of sulfonyl chlorides, proper handling and storage are essential to avoid hydrolysis and ensure safety, as they can release hydrochloric acid upon reaction with water.
Formula:C7H6ClFO2S
InChI:InChI=1/C7H6ClFO2S/c1-5-4-6(12(8,10)11)2-3-7(5)9/h2-4H,1H3
SMILES:Cc1cc(ccc1F)S(=O)(=O)Cl
Synonyms:- 4-Fluor-3-methylbenzolsulfonylchlorid
- Benzenesulfonyl chloride, 4-fluoro-3-methyl-
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Found 3 products.
4-Fluoro-3-methylbenzenesulfonyl chloride
CAS:Formula:C7H6ClFO2SPurity:97%Color and Shape:LiquidMolecular weight:208.63774-Fluoro-3-methylbenzenesulphonyl chloride
CAS:<p>4-Fluoro-3-methylbenzenesulphonyl chloride</p>Purity:≥95%Color and Shape:SolidMolecular weight:208.64g/mol4-Fluoro-3-methylbenzenesulfonyl chloride
CAS:Formula:C7H6ClFO2SPurity:97%(GC-MS);RGColor and Shape:ClearMolecular weight:208.63


