Ethyl 3-amino-5-chloro-1H-indole-2-carboxylate is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This compound features an ethyl ester functional group, an amino group, and a chlorine substituent, contributing to its reactivity and potential biological activity. The presence of the amino group suggests that it may participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions. The chlorine atom can influence the compound's electronic properties and steric hindrance, potentially affecting its interaction with biological targets. Ethyl 3-amino-5-chloro-1H-indole-2-carboxylate may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural features that can mimic natural compounds. Additionally, its solubility and stability in various solvents can be important for its application in synthetic processes or as a research reagent. Overall, this compound exemplifies the complexity and diversity of indole derivatives in organic chemistry.

ethyl 3-amino-5-chloro-1H-indole-2-carboxylate

62578-58-9: Ethyl 3-amino-5-chloro-1H-indole-2-carboxylate is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This compound features an ethyl ester functional group, an amino group, and a chlorine substituent, contributing to its reactivity and potential biological activity. The presence of the amino group suggests that it may participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions. The chlorine atom can influence the compound's electronic properties and steric hindrance, potentially affecting its interaction with biological targets. Ethyl 3-amino-5-chloro-1H-indole-2-carboxylate may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural features that can mimic natural compounds. Additionally, its solubility and stability in various solvents can be important for its application in synthetic processes or as a research reagent. Overall, this compound exemplifies the complexity and diversity of indole derivatives in organic chemistry.

CAS 62578-58-9

ethyl 3-amino-5-chloro-1H-indole-2-carboxylate

Ethyl 3-amino-5-chloro-1H-indole-2-carboxylate

Ref: IN-DA00EKVU

Ethyl 3-amino-5-chloro-1H-indole-2-carboxylate

Ref: 54-OR45004