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CAS 3636-65-5

:

ethyl [(4-chlorophenyl)sulfonyl]acetate

Description:
Ethyl [(4-chlorophenyl)sulfonyl]acetate, with the CAS number 3636-65-5, is an organic compound characterized by its sulfonyl functional group attached to an ethyl acetate moiety. This compound features a 4-chlorophenyl group, which contributes to its chemical reactivity and potential applications in various chemical reactions, particularly in organic synthesis. The presence of the sulfonyl group enhances its electrophilic character, making it useful in nucleophilic substitution reactions. Ethyl [(4-chlorophenyl)sulfonyl]acetate is typically a colorless to pale yellow liquid, exhibiting moderate solubility in organic solvents. It is important to handle this compound with care, as it may pose health risks if inhaled or ingested, and appropriate safety measures should be taken during its use in laboratory settings. Its applications may include serving as an intermediate in the synthesis of pharmaceuticals or agrochemicals, highlighting its significance in the field of medicinal chemistry and material science.
Formula:C10H11ClO4S
InChI:InChI=1/C10H11ClO4S/c1-2-15-10(12)7-16(13,14)9-5-3-8(11)4-6-9/h3-6H,2,7H2,1H3
SMILES:CCOC(=O)CS(=O)(=O)c1ccc(cc1)Cl
Synonyms:
  • Acetic acid, [(4-chlorophenyl)sulfonyl]-, ethyl ester
  • Acetic acid, [(p-chlorophenyl)sulfonyl]-, ethyl ester
  • Acetic Acid, 2-[(4-Chlorophenyl)Sulfonyl]-, Ethyl Ester
  • Ethyl [(4-chlorophenyl)sulfonyl]acetate
  • [(4-Chlorophenyl)sulfonyl]acetic acid ethyl ester
  • ETHYL 2-[(4-CHLOROPHENYL)SULPHONYL]ACETATE
  • Ethyl 2-[(4-chlorophenyl)sulphonyl]ethanoate, 4-Chlorophenyl 2-ethoxy-2-oxoethyl sulphone
  • ETHYL[(4-CHLOROPHENYL)SULPHONYL]ACETATE
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