Ethyl 4-{[(2-chloroethyl)carbamoyl]amino}benzoate, with the CAS number 13908-47-9, is a chemical compound that belongs to the class of benzoate esters. It features a benzoate moiety substituted with an ethyl group and a 2-chloroethyl carbamoyl amino group, which contributes to its unique reactivity and potential biological activity. This compound is characterized by its moderate polarity, which influences its solubility in organic solvents and water. The presence of the chloroethyl group suggests potential for nucleophilic substitution reactions, making it a candidate for further chemical transformations. Additionally, the carbamoyl group may impart certain pharmacological properties, indicating potential applications in medicinal chemistry. Ethyl 4-{[(2-chloroethyl)carbamoyl]amino}benzoate may also exhibit specific interactions with biological targets, which could be of interest in drug development. However, detailed studies on its toxicity, stability, and specific applications are necessary to fully understand its characteristics and potential uses in various fields, including pharmaceuticals and agrochemicals.

ethyl 4-{[(2-chloroethyl)carbamoyl]amino}benzoate

13908-47-9: Ethyl 4-{[(2-chloroethyl)carbamoyl]amino}benzoate, with the CAS number 13908-47-9, is a chemical compound that belongs to the class of benzoate esters. It features a benzoate moiety substituted with an ethyl group and a 2-chloroethyl carbamoyl amino group, which contributes to its unique reactivity and potential biological activity. This compound is characterized by its moderate polarity, which influences its solubility in organic solvents and water. The presence of the chloroethyl group suggests potential for nucleophilic substitution reactions, making it a candidate for further chemical transformations. Additionally, the carbamoyl group may impart certain pharmacological properties, indicating potential applications in medicinal chemistry. Ethyl 4-{[(2-chloroethyl)carbamoyl]amino}benzoate may also exhibit specific interactions with biological targets, which could be of interest in drug development. However, detailed studies on its toxicity, stability, and specific applications are necessary to fully understand its characteristics and potential uses in various fields, including pharmaceuticals and agrochemicals.

CAS 13908-47-9

ethyl 4-{[(2-chloroethyl)carbamoyl]amino}benzoate

Benzoic acid, 4-[[[(2-chloroethyl)amino]carbonyl]amino]-, ethyl ester

Ref: IN-DA001A7A

Ethyl 4-(2-chloroethylcarbamoylamino)benzoate

Ref: 54-OR47838