CAS 6915-67-9
:3-phenyl-1H-indole-2-carboxylic acid
Description:
3-Phenyl-1H-indole-2-carboxylic acid is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a phenyl group at the 3-position and a carboxylic acid functional group at the 2-position contributes to its unique chemical properties. This compound typically exhibits moderate solubility in organic solvents and may have limited solubility in water due to the hydrophobic nature of the indole ring. It can participate in various chemical reactions, including acid-base reactions, due to the carboxylic acid group, and can also engage in hydrogen bonding. The compound is of interest in medicinal chemistry and research due to its potential biological activities, including anti-inflammatory and anticancer properties. Its molecular structure allows for interactions with biological targets, making it a subject of study in drug development. As with many organic compounds, proper handling and safety precautions are essential when working with 3-phenyl-1H-indole-2-carboxylic acid in laboratory settings.
Formula:C15H11NO2
InChI:InChI=1/C15H11NO2/c17-15(18)14-13(10-6-2-1-3-7-10)11-8-4-5-9-12(11)16-14/h1-9,16H,(H,17,18)
SMILES:c1ccc(cc1)c1c2ccccc2[nH]c1C(=O)O
Synonyms:- 1H-indole-2-carboxylic acid, 3-phenyl-
- 3-PHENYL-1H-INDOLE-2-CARBOXYLIC ACID
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Found 2 products.
3-Phenyl-1H-indole-2-carboxylic Acid
CAS:<p>3-Phenyl-1H-indole-2-carboxylic acid is a chemical compound that has an acidic property. It is used in the analysis of hormones, such as testosterone and estradiol. 3-Phenyl-1H-indole-2-carboxylic acid is used to analyze the biotic and abiotic properties of a sample by liquid chromatography. It can be used for the profiling of steroids, such as cortisol and cortisone, and sex hormones. This chemical is also used to highlight the presence of acetonitrile in a sample.</p>Formula:C15H11NO2Purity:Min. 95%Molecular weight:237.25 g/mol
