3-Quinolinecarboxaldehyde TCI Q0075

Chemical Identity

CAS No.: 13669-42-6
PubChem: CID 83641·SID 87561545
Formula: C10H7NO
Molecular weight: 157.17 g/mol
Purity: >96.0%(GC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: quinoline-3-carbaldehyde
SMILES: C1=CC=C2C(=C1)C=C(C=N2)C=O
InChIKey: RYGIHSLRMNXWCN-UHFFFAOYSA-N

Rp 2.677.500,00

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3-Quinolinecarboxaldehyde is a chemical compound widely used as a building block in the synthesis of heterocyclic compounds. Its molecular structure consists of a quinoline ring linked to an aldehyde group, making it a versatile intermediate in organic chemistry. In laboratory settings, this compound plays a crucial role in creating complex molecular structures with diverse applications in pharmaceutical, material, and organic chemistry research. Due to its structural complexity and functional group, it is a key component in various synthetic pathways.

The compound is valued for its stable chemical structure and controlled reactivity, which make it suitable for a range of chemical reactions. It exhibits good compatibility with various reagents such as amines, alcohols, and carboxylic acids, enabling the formation of new chemical entities. Its predictable behavior in reactions like condensation, nucleophilic substitution, and electrophilic addition makes it a preferred choice for synthetic chemists. These properties ensure consistent results and reliability in laboratory experiments.

In Indonesian laboratories, 3-Quinolinecarboxaldehyde is commonly used in scientific research and chemical product development. It is integral to projects involving the synthesis of new compounds, drug development, and material characterization. Many research institutions and universities in Indonesia rely on this compound for advancing their studies in organic chemistry and pharmaceutical sciences. Its widespread use underscores its importance in both academic and industrial research contexts.

Related TCI products

Synthesis of heterocyclic compounds for pharmaceutical development due to its reactive aldehyde group and quinoline ring.
Organic reaction studies involving nucleophilic and electrophilic substitution due to its stable molecular structure.
Drug discovery projects where complex molecular frameworks are required for bioactive molecule design.
Material characterization experiments requiring functionalized aromatic compounds for polymer synthesis.
Academic research in organic chemistry for teaching and experimental methodology development.

Brand	TCI
CAS number	13669-42-6
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid
Storage	Store in a cool, dry place away from light

3-Quinolinecarboxaldehyde should be stored in a cool, dry place, away from direct light and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. As a solid, it is typically handled using standard laboratory equipment, with care taken to avoid exposure to incompatible substances. Proper ventilation is advised during handling to minimize inhalation risks. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, when working with this compound. Regular inspection of storage conditions ensures the compound remains stable and suitable for use in chemical synthesis and research applications.

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