CAS 82717-40-6
:1H-Indole-2-carboxylicacid, octahydro-
Description:
1H-Indole-2-carboxylic acid, octahydro- (CAS 82717-40-6) 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 specific derivative features a carboxylic acid functional group at the 2-position of the indole ring, contributing to its acidic properties. The "octahydro-" prefix indicates that the compound has undergone hydrogenation, resulting in a saturated structure that may influence its reactivity and solubility. Typically, compounds of this nature are of interest in medicinal chemistry due to their potential biological activities, including antimicrobial and anti-inflammatory properties. The presence of the carboxylic acid group enhances its ability to participate in hydrogen bonding, which can affect its interactions with biological targets. Additionally, the compound's molecular weight, melting point, and solubility characteristics would be relevant for applications in pharmaceuticals or organic synthesis, although specific values would need to be referenced from experimental data.
Formula:C9H15NO2
Synonyms:- 1H-Indole-2-carboxylicacid,octahydro-(9CI)
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Found 1 products.
D-Octahydroindole-2-carboxylic acid
CAS:<p>D-Octahydroindole-2-carboxylic acid is a hydrogen chloride salt of D-octahydroindole-2-carboxylic acid. It is an opioid receptor agonist with a δ affinity, and has been shown to inhibit thrombin. D-Octahydroindole-2-carboxylic acid has also been shown to have anti-cancer properties, inhibiting the growth of cancer cells by blocking the production of prostaglandins. It has also been found to reduce blood pressure in rats by inhibiting the enzyme responsible for the conversion of angiotensin I into angiotensin II.</p>Formula:C9H15NO2Purity:Min. 95%Molecular weight:169.22 g/mol
