CAS 24985-85-1
:Ethyl 5-hydroxy-1H-indole-2-carboxylate
Description:
Ethyl 5-hydroxy-1H-indole-2-carboxylate, identified by its CAS number 24985-85-1, is an organic compound that belongs to the indole family, characterized by its bicyclic structure comprising a benzene ring fused to a pyrrole ring. This compound features a carboxylate ester functional group, which contributes to its reactivity and solubility properties. The presence of a hydroxyl group at the 5-position enhances its potential for hydrogen bonding, influencing its solubility in polar solvents and its biological activity. Ethyl 5-hydroxy-1H-indole-2-carboxylate is of interest in various fields, including medicinal chemistry, due to its potential pharmacological properties. It may exhibit antioxidant, anti-inflammatory, or other biological activities, making it a candidate for further research in drug development. Additionally, its structural characteristics allow for various synthetic modifications, which can lead to the development of derivatives with enhanced efficacy or selectivity. As with many indole derivatives, it may also participate in various chemical reactions, including electrophilic substitutions and condensation reactions.
Formula:C11H11NO3
InChI:InChI=1S/C11H11NO3/c1-2-15-11(14)10-6-7-5-8(13)3-4-9(7)12-10/h3-6,12-13H,2H2,1H3
InChI key:InChIKey=WANAXLMRGYGCPC-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C1=CC=2C(N1)=CC=C(O)C2
Synonyms:- (1-Benzylpiperidin-3-Yl)Methanol
- 1H-Indole-2-carboxylic acid, 5-hydroxy-, ethyl ester
- 5-Hydroxy-1H-indole-2-carboxylic acid ethyl ester
- 5-Hydroxyindole-2-carboxylic acid ethyl ester
- Indole-2-carboxylic acid, 5-hydroxy-, ethyl ester
- ethyl 5-hydroxy-1H-indole-2-carboxylate
- Ethyl 5-hydroxyindole-2-carboxylate
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Found 6 products.
Ethyl 5-hydroxyindole-2-carboxylate, 98+%
CAS:<p>Ethyl 5-hydroxyindole-2-carboxylate is used as an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and Dyestuffs. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label info</p>Formula:C11H11NO3Purity:98+%Color and Shape:Crystals or powder or crystalline powder or lumps or fused solid or granules, White to cream to brown or pink to grayMolecular weight:205.211H-Indole-2-carboxylic acid, 5-hydroxy-, ethyl ester
CAS:Formula:C11H11NO3Purity:97%Color and Shape:SolidMolecular weight:205.2099Ethyl 5-hydroxyindole-2-carboxylate
CAS:<p>Ethyl 5-hydroxyindole-2-carboxylate</p>Purity:99%Molecular weight:205.21g/mol5-Hydroxyindole-2-carboxylic acid ethyl ester
CAS:<p>5-Hydroxyindole-2-carboxylic acid ethyl ester is a fluorescent probe that is used in the detection of hepatitis C virus by micropet assay. The compound reacts with amines and undergoes fluorescence quenching, and can be used to quantitate their concentration. 5-Hydroxyindole-2-carboxylic acid ethyl ester is also used for the determination of the kinetics of amines and other compounds that are involved in the metabolism of drugs and biogenic amines. It can be applied to chromatographic analysis or sample preparation prior to analysis by analytical chemistry methods such as gas chromatography or liquid chromatography.</p>Formula:C11H11NO3Purity:Min. 95%Color and Shape:PowderMolecular weight:205.21 g/mol5-Hydroxy-1H-indole-2-carboxylic acid ethyl ester
CAS:Formula:C11H11NO3Purity:97%Color and Shape:SolidMolecular weight:205.2135-Hydroxyindole-2-carboxylic acid ethyl ester
CAS:<p>5-Hydroxyindole-2-carboxylic acid ethyl ester is a fine chemical that is used as a building block for complex compounds. It has been shown to react with nucleophiles to form five-membered heterocycles, which can be used as reaction components or intermediates in the synthesis of more complex molecules. 5-Hydroxyindole-2-carboxylic acid ethyl ester is versatile and can be modified to create new scaffolds for drug discovery. The compound is readily available and has high quality, making it an excellent choice for research purposes.</p>Formula:C11H11NO3Purity:Min. 99 Area-%Molecular weight:205.22 g/mol




