CAS 486-74-8

4-Quinolinecarboxylic acid

Description:

4-Quinolinecarboxylic acid, with the CAS number 486-74-8, is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. This compound features a carboxylic acid functional group (-COOH) at the 4-position of the quinoline ring, contributing to its acidic properties. It is typically a white to light yellow crystalline solid that is soluble in polar solvents like water and alcohols, while being less soluble in non-polar solvents. The presence of the carboxylic acid group allows it to participate in various chemical reactions, including esterification and amidation. 4-Quinolinecarboxylic acid is of interest in medicinal chemistry and materials science due to its potential biological activities, including antimicrobial and anti-inflammatory properties. Additionally, it can serve as a precursor for the synthesis of various derivatives, which may exhibit enhanced pharmacological effects. Its stability and reactivity make it a valuable compound in both research and industrial applications.

Formula: C₁₀H₇NO₂

InChI: InChI=1S/C10H7NO2/c12-10(13)8-5-6-11-9-4-2-1-3-7(8)9/h1-6H,(H,12,13)

InChI key: InChIKey=VQMSRUREDGBWKT-UHFFFAOYSA-N

SMILES: C(O)(=O)C=1C2=C(N=CC1)C=CC=C2

Synonyms:

• 4-Carboxyquinoline
• 4-Quinolinecarboxylic acid
• 4-Quinolinic acid
• Cinchoninic acid
• Cinnchoninic Acid
• N-Quinoline-4-carboxylic acid
• NSC 13138
• Quinoline-4-Carboxylate

4-Quinolinecarboxylic Acid

CAS: 486-74-8

Formula: C₁₀H₇NO₂

Purity: >98.0%(T)(HPLC)

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 173.17

Ref: 3B-Q0065

Quinoline-4-carboxylic acid, 98+%

CAS: 486-74-8

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₁₀H₇NO₂

Purity: 98+%

Molecular weight: 173.17

Ref: 02-L14611

Quinoline-4-carboxylic acid

CAS: 486-74-8

Formula: C₁₀H₇NO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 173.1681

Ref: IN-DA00DECO

Quinoline-4-carboxylic acid

CAS: 486-74-8

Quinoline-4-carboxylic acid

Formula: C₁₀H₇NO₂

Purity: ≥95%

Color and Shape: light brown powder

Molecular weight: 173.17g/mol

Ref: 54-OR0731

Quinoline-4-carboxylic acid

CAS: 486-74-8

Formula: C₁₀H₇NO₂

Molecular weight: 173.17

Ref: 7W-GK8917

4-Carboxyquinoline

CAS: 486-74-8

4-Carboxyquinoline

Purity: ≥98%

Molecular weight: 173.17g/mol

Ref: 54-BUP17917

4-Carboxyquinoline

CAS: 486-74-8

4-Carboxyquinoline (4-Quinolinecarboxylic acid) showed anti-tumor activity against L1210 leukemia and B16 melanoma.

Formula: C₁₀H₇NO₂

Purity: 99.46% - 99.69%

Color and Shape: White To Light Yellow Crystal Powder

Molecular weight: 173.17

Ref: TM-T4745

Quinoline-4-carboxylic acid

CAS: 486-74-8

Formula: C₁₀H₇NO₂

Purity: 97%

Color and Shape: Solid, Light brown powder

Molecular weight: 173.171

Ref: 10-F066325

Quinoline-4-carboxylic Acid

Controlled Product

CAS: 486-74-8

Applications Quinoline-4-carboxylic acid (cas# 486-74-8) is a useful research chemical.

Formula: C₁₀H₇NO₂

Color and Shape: Neat

Molecular weight: 173.16

Ref: TR-Q700508

Quinoline-4-carboxylic acid

CAS: 486-74-8

Quinoline-4-carboxylic acid is a natural compound that is derived from the amino acid tryptophan. It has been shown to have antiinflammatory activity and to be an inhibitor of prostaglandin synthesis. Quinoline-4-carboxylic acid inhibits the growth of carcinoma cells in culture by inducing apoptosis, which is mediated by inhibition of protein synthesis. Quinoline-4-carboxylic acid also has pharmacokinetic properties, including a low volume of distribution, low clearance rate and high bioavailability.

Formula: C₁₀H₇NO₂

Purity: Min. 97 Area-%

Molecular weight: 173.17 g/mol

Ref: 3D-FQ31508