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CAS 501697-77-4

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4-(3,4-dichlorophenoxy)benzenesulfonyl chloride

Description:
4-(3,4-Dichlorophenoxy)benzenesulfonyl chloride is a chemical compound characterized by its sulfonyl chloride functional group, which is known for its reactivity and utility in organic synthesis. This compound features a dichlorophenoxy group, indicating the presence of two chlorine atoms on the phenyl ring, which can influence its electronic properties and reactivity. The sulfonyl chloride moiety makes it a potent electrophile, allowing it to participate in nucleophilic substitution reactions, particularly with amines and alcohols, to form sulfonamides and sulfonates, respectively. The presence of chlorine substituents can enhance the compound's lipophilicity and may affect its biological activity. This compound is typically used in the synthesis of various pharmaceuticals and agrochemicals, owing to its ability to introduce sulfonyl groups into organic molecules. As with many sulfonyl chlorides, it is important to handle this compound with care due to its potential reactivity and the release of hydrochloric acid upon hydrolysis. Proper safety measures should be observed when working with this substance in a laboratory setting.
Formula:C12H7Cl3O3S
InChI:InChI=1/C12H7Cl3O3S/c13-11-6-3-9(7-12(11)14)18-8-1-4-10(5-2-8)19(15,16)17/h1-7H
SMILES:c1cc(ccc1Oc1ccc(c(c1)Cl)Cl)S(=O)(=O)Cl
Synonyms:
  • Benzenesulfonyl chloride, 4-(3,4-dichlorophenoxy)-
  • 4-(3,4-Dichlorophenoxy)benzenesulfonyl chloride
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