Ethyl 3-[3-(4-methylsulfanylphenyl)propanoyl]benzoate, identified by its CAS number 898780-95-5, is an organic compound characterized by its ester functional group, which is derived from benzoic acid and an ethyl alcohol moiety. This compound features a complex structure that includes a benzoate moiety, a propanoyl group, and a methylsulfanyl substituent on the phenyl ring, contributing to its unique chemical properties. The presence of the methylsulfanyl group enhances its potential for biological activity, possibly influencing its solubility and reactivity. Ethyl esters like this one are often used in organic synthesis and may exhibit interesting pharmacological properties. The compound's molecular structure suggests it may participate in various chemical reactions, including esterification and nucleophilic substitutions. Its specific characteristics, such as melting point, boiling point, and solubility, would depend on the molecular interactions and the environment in which it is studied. Overall, this compound represents a fascinating example of how structural modifications can lead to diverse chemical behaviors and potential applications in medicinal chemistry.

ethyl 3-[3-(4-methylsulfanylphenyl)propanoyl]benzoate

898780-95-5: Ethyl 3-[3-(4-methylsulfanylphenyl)propanoyl]benzoate, identified by its CAS number 898780-95-5, is an organic compound characterized by its ester functional group, which is derived from benzoic acid and an ethyl alcohol moiety. This compound features a complex structure that includes a benzoate moiety, a propanoyl group, and a methylsulfanyl substituent on the phenyl ring, contributing to its unique chemical properties. The presence of the methylsulfanyl group enhances its potential for biological activity, possibly influencing its solubility and reactivity. Ethyl esters like this one are often used in organic synthesis and may exhibit interesting pharmacological properties. The compound's molecular structure suggests it may participate in various chemical reactions, including esterification and nucleophilic substitutions. Its specific characteristics, such as melting point, boiling point, and solubility, would depend on the molecular interactions and the environment in which it is studied. Overall, this compound represents a fascinating example of how structural modifications can lead to diverse chemical behaviors and potential applications in medicinal chemistry.

CAS 898780-95-5

ethyl 3-[3-(4-methylsulfanylphenyl)propanoyl]benzoate

3′-carboethoxy-3-(4-thiomethylphenyl)propiophenone

Ref: 10-F205999