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TCI

CAS 6480-68-8

3-Quinolinecarboxylic Acid TCI Q0090

3-Quinolinecarboxylic Acid TCI Q0090

Chemical Identity

CAS No.
6480-68-8
PubChem
CID 80971·SID 253662064
Formula
C10H7NO2
Molecular weight
173.17 g/mol
Purity
>98.0%(HPLC)(T)
Reference databases
ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
quinoline-3-carboxylic acid
SMILES
C1=CC=C2C(=C1)C=C(C=N2)C(=O)O
InChIKey
DJXNJVFEFSWHLY-UHFFFAOYSA-N
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3-Quinolinecarboxylic Acid is a chemical compound with a heterocyclic structure, featuring a quinoline ring and a carboxylic acid group at the third position. This compound plays a crucial role in laboratory settings, particularly in the synthesis of complex molecules. It serves as a fundamental building block in organic chemistry and pharmacology, enabling the development of compounds with specific biological activities. Its versatility makes it an essential tool for researchers and students engaged in chemical synthesis and drug discovery.

The compound exhibits chemical stability and moderate reactivity, making it suitable for various synthetic reactions such as esterification, amidation, and substitution reactions. These properties contribute to its popularity among chemists seeking reliable and effective reagents. Additionally, its good solubility in organic solvents simplifies processing and separation techniques in the laboratory, enhancing the efficiency of experimental workflows.

In Indonesian laboratories, 3-Quinolinecarboxylic Acid is widely utilized by researchers and students in diverse chemical studies. It frequently appears in projects related to drug development, organic synthesis, and analytical chemistry. Its availability and consistent performance make it a preferred choice for both academic and industrial research applications in the region.

  • Organic synthesis: This compound is widely used in the synthesis of complex organic molecules due to its reactivity and structural versatility.
  • Pharmaceutical research: It serves as a key building block in the development of pharmaceutical compounds with specific biological activities.
  • Analytical chemistry: Its solubility and chemical stability make it suitable for use in analytical procedures and chromatographic analyses.
  • Drug discovery: Researchers use it to design and test new drug candidates with targeted therapeutic effects.
  • Teaching and research in universities: It is commonly used in academic settings to support both undergraduate and graduate-level chemical experiments.

Brand TCI
CAS number 6480-68-8
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply options
Physical form Solid
Storage Store in a cool, dry place away from direct sunlight and moisture

3-Quinolinecarboxylic Acid should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in airtight containers to prevent exposure to moisture and air. The compound should be stored away from direct sunlight and sources of heat to avoid degradation. In laboratory settings, it is important to handle the material with appropriate personal protective equipment, such as gloves and safety goggles. Proper ventilation should be ensured when working with this compound to minimize inhalation risks. Regular monitoring of storage conditions ensures the compound remains effective and safe for use in research applications.

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