CAS 93-10-7

Quinaldic acid

Description:

Quinaldic acid, with the CAS number 93-10-7, is an organic compound that belongs to the class of amino acids and is characterized by its aromatic structure. It is a derivative of quinoline, featuring a carboxylic acid group and an amino group, which contributes to its acidic properties. Quinaldic acid is typically a white to pale yellow crystalline solid that is soluble in water and organic solvents, making it versatile for various applications. Its molecular formula is C10H9NO2, and it has a melting point that varies depending on purity and specific conditions. This compound is primarily used in the synthesis of dyes, pharmaceuticals, and agrochemicals, owing to its ability to participate in various chemical reactions, including condensation and substitution reactions. Additionally, quinaldic acid exhibits biological activity, which has led to research into its potential therapeutic applications. Overall, its unique structure and reactivity make quinaldic acid an important compound in both industrial and research settings.

Formula: C₁₀H₇NO₂

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

InChI key: InChIKey=LOAUVZALPPNFOQ-UHFFFAOYSA-N

SMILES: C(O)(=O)C1=NC2=C(C=C1)C=CC=C2

Synonyms:

• 2-Carboxyl Quinoline
• 2-Carboxyquinoline
• 2-Quinoline carboxylic Acid
• 2-Quinolinecarbocylic Acid
• 2-Quinolinecarboxylic acid
• 2-Quinolinic acid
• 2-Quinolinylcarboxylic acid
• Acide quinoleine-2-carboxylique
• Acido Quinolina-2-Carboxilico
• Akos Bbs-00003779
• Chinolin-2-carbonsaure
• Nsc 4882
• Quinaldinic Acid
• Quinolin-2-carboxylic acid
• Quinoline-2-Carboxylate
• Quinoline-2-carboxylic Acid
• Quinoline-2-carboxylic acid (Quinaldic acid)
• Rarechem Al Bo 1348
• Timtec-Bb Sbb003820

Quinaldic Acid

CAS: 93-10-7

Formula: C₁₀H₇NO₂

Purity: >98.0%(T)(HPLC)

Color and Shape: White to Orange to Green powder to crystal

Molecular weight: 173.17

Ref: 3B-Q0003

Quinaldic acid, 98%

CAS: 93-10-7

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%

Color and Shape: White to cream or pale yellow or pale brown, Crystals or powder or crystalline powder

Molecular weight: 173.17

Ref: 02-A10192

Quinoline-2-carboxylic acid, 10mM (in DMSO)

CAS: 93-10-7

Quinoline-2-carboxylic acid, 10mM (in DMSO)

Purity: ≥98%

Molecular weight: 173.17g/mol

Ref: 54-BUP19940

Quinoline-2-carboxylic acid

CAS: 93-10-7

Quinoline-2-carboxylic acid

Purity: ≥98%

Molecular weight: 173.17g/mol

Ref: 54-BUP19048

Quinoline-2-carboxylic acid

CAS: 93-10-7

Quinoline-2-carboxylic acid (RARECHEM AL BO 1348) belongs to the class of organic compounds known as quinoline carboxylic acids.

Formula: C₁₀H₇NO₂

Purity: 99.49% - 99.92%

Color and Shape: Solid

Molecular weight: 173.17

Ref: TM-T4780

Quinoline-2-carboxylic acid

CAS: 93-10-7

Quinoline-2-carboxylic acid

Formula: C₁₀H₇NO₂

Purity: 99%

Color and Shape: pale yellow solid

Molecular weight: 173.17g/mol

Ref: 54-OR23072

Quinaldic acid

CAS: 93-10-7

Formula: C₁₀H₇NO₂

Purity: ≥ 98.0%

Color and Shape: White to yellow powder or crystals

Molecular weight: 173.17

Ref: 7W-GK8424

2-Quinolinecarboxylic acid

CAS: 93-10-7

2-Quinolinecarboxylic acid is an antibiotic that is used in the treatment of bacterial infections and has inhibitory properties. It has been shown to be a competitive inhibitor of the enzyme quinolinate phosphoribosyltransferase, which catalyzes the conversion of quinolinic acid to nicotinic acid. 2-Quinolinecarboxylic acid binds to the active site of the enzyme and prevents substrate binding, thereby blocking the production of nicotinic acid. This drug also inhibits bacterial growth by binding to DNA-dependent RNA polymerase, thereby preventing transcription and replication. The high frequency of human activity has been shown using a patch-clamp technique on human erythrocytes. This active form is metabolized through a number of metabolic transformations, including hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucur

Formula: C₁₀H₇NO₂

Purity: Min. 98 Area-%

Color and Shape: Powder

Molecular weight: 173.17 g/mol

Ref: 3D-FQ10003

2-Quinolinecarboxylic acid

CAS: 93-10-7

Formula: C₁₀H₇NO₂

Purity: 98%

Color and Shape: Solid, White powder

Molecular weight: 173.171

Ref: 10-F036133

2-​Quinolinecarboxylic Acid

Controlled Product

CAS: 93-10-7

Applications 2-​Quinolinecarboxylic acid can be found in the studying of ligands for the purpose of copper-catalyzed Ullmann reactions with aryl ethers and aryl iodides.

Formula: C₁₀H₇NO₂

Color and Shape: Neat

Molecular weight: 173.17

Ref: TR-Q700490