CAS 53951-84-1
:methyl quinoline-3-carboxylate
Description:
Methyl quinoline-3-carboxylate is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. This compound features a carboxylate functional group (-COO-) attached to the third position of the quinoline ring, along with a methyl group (-CH3) esterified to the carboxylic acid. It typically appears as a yellow to brown solid or liquid, depending on its purity and specific conditions. Methyl quinoline-3-carboxylate is known for its potential applications in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to the biological activity associated with quinoline derivatives. The compound may exhibit various chemical properties, including solubility in organic solvents and reactivity towards nucleophiles, making it a versatile intermediate in chemical reactions. Additionally, its structure allows for potential interactions with biological systems, which can be explored in medicinal chemistry. Safety data should be consulted for handling and storage, as with any chemical substance.
Formula:C11H9NO2
InChI:InChI=1/C11H9NO2/c1-14-11(13)9-6-8-4-2-3-5-10(8)12-7-9/h2-7H,1H3
SMILES:COC(=O)c1cc2ccccc2nc1
Synonyms:- methyl quinoline-3-carboxylate
- Methyl 3-quinolinecarboxylate
- 3-Quinolinecarboxylic acid, methyl ester
- Quinoline-3-carboxylic acid methyl ester
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Found 4 products.
Methyl quinoline-3-carboxylate
CAS:Formula:C11H9NO2Purity:97%Color and Shape:SolidMolecular weight:187.1947Methyl quinoline-3-carboxylate
CAS:Methyl quinoline-3-carboxylatePurity:95%Molecular weight:187.19g/molMethyl quinoline-3-carboxylate
CAS:Formula:C11H9NO2Purity:97%Color and Shape:SolidMolecular weight:187.198Methyl quinoline-3-carboxylate
CAS:<p>Methyl quinoline-3-carboxylate is a methyl ester of quinoline-3-carboxylic acid. It is used in the synthesis of quinoline, which is an organic compound that has been shown to have antiarrhythmic and antithrombotic effects. Methyl quinoline-3-carboxylate has been shown to be effective against tuberculosis bacteria through its interaction with the cellular membrane and inhibition of nitrosation reactions. This drug also has been studied for its potential use as a treatment for heart diseases due to its ability to inhibit oxidation reactions.</p>Formula:C11H9NO2Purity:Min. 95%Molecular weight:187.2 g/mol



