3-(Ethylsulfanyl)benzoic acid, with the CAS number 5537-74-6, is an organic compound characterized by the presence of a benzoic acid moiety substituted with an ethylsulfanyl group at the meta position. This compound features a carboxylic acid functional group (-COOH), which imparts acidic properties, making it soluble in polar solvents and capable of participating in acid-base reactions. The ethylsulfanyl group (-S-ethyl) contributes to the compound's unique reactivity and potential for forming various derivatives. The presence of the sulfur atom can enhance the compound's nucleophilicity and influence its interactions with other chemical species. Additionally, the aromatic nature of the benzene ring provides stability and can facilitate π-π stacking interactions in solid-state or solution environments. The compound may exhibit biological activity, making it of interest in pharmaceutical research. Its physical properties, such as melting point and boiling point, would depend on the specific molecular interactions and the presence of functional groups. Overall, 3-(ethylsulfanyl)benzoic acid is a versatile compound with potential applications in organic synthesis and medicinal chemistry.

3-(ethylsulfanyl)benzoic acid

5537-74-6: 3-(Ethylsulfanyl)benzoic acid, with the CAS number 5537-74-6, is an organic compound characterized by the presence of a benzoic acid moiety substituted with an ethylsulfanyl group at the meta position. This compound features a carboxylic acid functional group (-COOH), which imparts acidic properties, making it soluble in polar solvents and capable of participating in acid-base reactions. The ethylsulfanyl group (-S-ethyl) contributes to the compound's unique reactivity and potential for forming various derivatives. The presence of the sulfur atom can enhance the compound's nucleophilicity and influence its interactions with other chemical species. Additionally, the aromatic nature of the benzene ring provides stability and can facilitate π-π stacking interactions in solid-state or solution environments. The compound may exhibit biological activity, making it of interest in pharmaceutical research. Its physical properties, such as melting point and boiling point, would depend on the specific molecular interactions and the presence of functional groups. Overall, 3-(ethylsulfanyl)benzoic acid is a versatile compound with potential applications in organic synthesis and medicinal chemistry.

CAS 5537-74-6

3-(ethylsulfanyl)benzoic acid

3-(Ethylsulfanyl)benzoic acid

Ref: IN-DA01A3HN

3-(Ethylsulfanyl)benzoic acid

Ref: 3D-FAA53774