CAS 20357-15-7
:1,2-Dimethylindole-3-carboxylic acid
Description:
1,2-Dimethylindole-3-carboxylic acid is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. This compound features two methyl groups attached to the first and second carbon atoms of the indole ring, along with a carboxylic acid functional group at the third position. The presence of these functional groups contributes to its chemical reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. The compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the carboxylic acid group. Its molecular structure allows for potential interactions with biological systems, making it of interest in medicinal chemistry. Additionally, 1,2-Dimethylindole-3-carboxylic acid may participate in various chemical reactions, such as esterification or amidation, which can be utilized in synthetic organic chemistry. Overall, this compound's unique structure and functional groups make it a valuable subject of study in both theoretical and applied chemistry.
Formula:C11H11NO2
InChI:InChI=1S/C11H11NO2/c1-7-10(11(13)14)8-5-3-4-6-9(8)12(7)2/h3-6H,1-2H3,(H,13,14)
InChI key:InChIKey=XYRXQPDMBJNYIU-UHFFFAOYSA-N
SMILES:C(O)(=O)C=1C=2C(N(C)C1C)=CC=CC2
Synonyms:- 1,2-Dimethyl-1H-indole-3-carboxylic acid
- 1,2-dimethyl-1H-indole-3-carboxylate
- 1H-Indole-3-carboxylic acid, 1,2-dimethyl-
- Indole-3-carboxylic acid, 1,2-dimethyl-
- 1,2-Dimethylindole-3-carboxylic acid
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Found 4 products.
1,2-Dimethyl-1H-indole-3-carboxylic acid
CAS:<p>1,2-Dimethyl-1H-indole-3-carboxylic acid</p>Purity:≥95%Color and Shape:PowderMolecular weight:189.21g/mol1,2-Dimethylindole-3-carboxylic acid
CAS:Formula:C11H11NO2Purity:95.0%Color and Shape:SolidMolecular weight:189.2141,2-Dimethylindole-3-carboxylicacid
CAS:Controlled Product<p>1,2-Dimethylindole-3-carboxylicacid is a synthetic compound that has been extensively screened for antiviral activity and found to be effective against hepatitis C virus. It inhibits HMG-CoA reductase by binding to the active site of the enzyme, inhibiting its ability to catalyze the conversion of HMG-CoA to mevalonate. This leads to reduced synthesis of sterols, which are necessary for lipid biosynthesis and cell membrane biogenesis. 1,2-Dimethylindole-3-carboxylicacid is stereoselectively active at the (R) enantiomer. The drug also has hepatoselective effects in animal models.<br>1,2-Dimethylindole-3-carboxylicacid is a linker analog of pyrazoles that have been shown to have antiinflammatory properties in human cells grown in culture. Efflux of this drug from cells may be due to increased</p>Formula:C11H11NO2Purity:Min. 95%Molecular weight:189.21 g/mol



