Ethyl 2,3-dihydro-1H-indole-2-carboxylate is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This substance features an ethyl ester functional group, contributing to its reactivity and solubility properties. The presence of the 2,3-dihydro configuration indicates that it has a saturated bond in the indole framework, which can influence its chemical behavior and stability. Typically, compounds like this may exhibit biological activity, making them of interest in medicinal chemistry and drug development. The molecular structure allows for potential interactions with various biological targets, and its ester functionality can undergo hydrolysis, making it relevant in synthetic organic chemistry. Additionally, the compound's CAS number, 50501-07-0, serves as a unique identifier for regulatory and safety information. Overall, ethyl 2,3-dihydro-1H-indole-2-carboxylate is a versatile compound with potential applications in various fields, including pharmaceuticals and agrochemicals.

ethyl 2,3-dihydro-1H-indole-2-carboxylate

50501-07-0: 1H-indole-2-carboxylic acid, 2,3-dihydro-, ethyl ester, Ethyl Indoline-2-carboxylate

Ethyl indoline-2-carboxylate is a hydrophobic molecule that has been shown to be a potent vasorelaxant agent. It is an analog of the indole-3-carboxylic acid and binds to the hydrophobic pocket of the L-type calcium channels. Ethyl indoline-2-carboxylate interacts with dicyclohexyl, an ion channel blocker, in order to produce its vasorelaxant effect. This drug also has an interaction with maldi-tof, which provides information about its molecular weight. The optical properties of ethyl indoline-2-carboxylate are unknown.

CAS 50501-07-0: ethyl 2,3-dihydro-1H-indole-2-carboxylate

Ethyl indoline-2-carboxylate

Ref: 3D-ACA50107

Ethyl indoline-2-carboxylate

Ref: IN-DA003R0C

Ethyl Indoline-2-carboxylate

Ref: 3B-I0595

Ethyl indoline-2-carboxylate

Ref: 54-OR940768

Ethyl indoline-2-carboxylate

Ref: 10-F689603