CAS 21233-61-4

methyl quinoline-4-carboxylate

Description:

Methyl quinoline-4-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 fourth position of the quinoline ring, along with a methyl group (-CH3) esterified to the carboxylic acid. Methyl quinoline-4-carboxylate is typically a yellow to brown solid or liquid, depending on its purity and specific conditions. It is known for its aromatic properties and can exhibit fluorescence. The compound is often used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to participate in various chemical reactions, such as nucleophilic substitutions and cyclizations. Additionally, it may possess biological activity, making it of interest in medicinal chemistry. As with many organic compounds, handling should be done with care, considering potential toxicity and environmental impact.

Formula: C₁₁H₉NO₂

InChI: InChI=1/C11H9NO2/c1-14-11(13)9-6-7-12-10-5-3-2-4-8(9)10/h2-7H,1H3

SMILES: COC(=O)c1ccnc2ccccc12

Synonyms:

• 4-Quinolinecarboxylic acid, methyl ester
• Methyl quinoline-4-carboxylate

Methyl quinoline-4-carboxylate

CAS: 21233-61-4

Formula: C₁₁H₉NO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 187.1947

Ref: IN-DA00BH2J

Methyl quinoline-4-carboxylate

CAS: 21233-61-4

Methyl quinoline-4-carboxylate

Purity: 97%

Molecular weight: 187.19g/mol

Ref: 54-OR955585

Methyl quinoline-4-carboxylate

CAS: 21233-61-4

Purity: 97%

Molecular weight: 187.197998

Ref: 10-F760208

Methyl quinoline-4-carboxylate (~90%)

Controlled Product

CAS: 21233-61-4

Applications Methyl quinoline-4-carboxylate (cas# 21233-61-4) is a useful research chemical.

Formula: C₁₁H₉NO₂

Purity: ~90%

Color and Shape: Neat

Molecular weight: 187.19

Ref: TR-M342353

Methyl quinoline-4-carboxylate

CAS: 21233-61-4

Methyl quinoline-4-carboxylate is a potent inhibitor of secretory phospholipase A2 (sPLA2), which is an enzyme that cleaves the fatty acid at the sn-2 position in phospholipids. It has been shown to inhibit sPLA2 activity in both nonpancreatic and pancreatic secretions, but not in plasma. Methyl quinoline-4-carboxylate also inhibits the functionalities of heterocycles, such as chromatographic and synthetic. Methyl quinoline-4-carboxylate can be synthesized by reacting an aldoxime with methyl 4-chloroquinoline carboxylate. The molecular ion of methyl quinoline-4-carboxylate has been observed at m/z 335, while its mass spectrum displays peaks at m/z 335, 319, and 307. This molecule is found in quinoline derivatives and aldox

Formula: C₁₁H₉NO₂

Purity: Min. 95%

Molecular weight: 187.2 g/mol

Ref: 3D-WAA23361