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CAS 374537-95-8

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Methyl 3-(4-chlorosulphonyl)phenylpropionate

Description:
Methyl 3-(4-chlorosulphonyl)phenylpropionate is an organic compound characterized by its ester functional group, which is derived from the reaction of a carboxylic acid and an alcohol. This compound features a propionate moiety linked to a phenyl ring that is substituted with a chlorosulfonyl group, which enhances its reactivity and potential applications in various chemical processes. The presence of the chlorosulfonyl group introduces both electron-withdrawing characteristics and potential for nucleophilic attack, making it useful in synthetic organic chemistry. The compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its unique structure suggests potential applications in pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis. Safety data should be consulted for handling, as compounds with sulfonyl and halogen substituents can pose health risks. Overall, Methyl 3-(4-chlorosulphonyl)phenylpropionate is a versatile compound with significant implications in chemical research and industry.
Formula:C10H11ClO4S
InChI:InChI=1/C10H11ClO4S/c1-15-10(12)7-4-8-2-5-9(6-3-8)16(11,13)14/h2-3,5-6H,4,7H2,1H3
SMILES:COC(=O)CCc1ccc(cc1)S(=O)(=O)Cl
Synonyms:
  • Methyl3-(4-chlorosulfonyl)phenylpropionate
  • Methyl 3-[4-(Chlorosulfonyl)Phenyl]Propanoate
  • 3-(4-Chlorosulfonylphenyl)propionic acid methyl ester
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