Indole-3-carboxaldehyde TCI I0027

Chemical Identity

CAS No.: 487-89-8
PubChem: CID 10256·SID 87571436
Formula: C9H7NO
Molecular weight: 145.16 g/mol
Purity: >98.0%(GC)
Reference databases: ChEBI·ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 1H-indole-3-carbaldehyde
SMILES: C1=CC=C2C(=C1)C(=CN2)C=O
InChIKey: OLNJUISKUQQNIM-UHFFFAOYSA-N

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Indole-3-carboxaldehyde is a chemical compound belonging to the heterocyclic category, characterized by its indole core structure extended with a carboxaldehyde group. This compound plays a crucial role in organic chemistry laboratories, serving as a fundamental building block for the synthesis of complex organic molecules. Its versatility makes it a valuable tool for researchers aiming to create new compounds through various chemical reactions, including condensation and substitution. In laboratory settings, it is widely used as a precursor in the development of pharmaceuticals, dyes, and other organic materials.

The compound’s chemical properties make it a preferred choice for laboratory applications. It exhibits stability under certain conditions, yet remains highly reactive, especially when interacting with other organic compounds. This reactivity is due to its complex molecular structure, which allows it to participate in a wide range of chemical transformations. Its sensitivity to moisture and UV light necessitates careful handling and storage, but these characteristics also contribute to its effectiveness in specialized synthetic processes.

In Indonesian laboratories, Indole-3-carboxaldehyde is commonly used in organic chemistry research, particularly in academic institutions and research centers. It is frequently applied in projects involving the synthesis of complex organic compounds, making it a staple in both educational and industrial research environments. Its role in advancing chemical research is well established, supporting a variety of scientific investigations.

Related TCI products

Organic synthesis projects benefit from this compound's reactivity and versatility in forming new chemical bonds.
Pharmaceutical research utilizes it as a building block for developing new drug compounds and bioactive molecules.
Dye and pigment synthesis relies on its ability to participate in condensation reactions that produce colored compounds.
Academic research in chemistry uses it to teach and demonstrate complex organic reaction mechanisms.
Industrial chemical processes incorporate it for the production of specialty chemicals and functional materials.

Brand	TCI
CAS number	487-89-8
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Solid or liquid depending on the specific formulation
Storage	Store in a cool, dry place away from light and moisture

Indole-3-carboxaldehyde should be stored in a cool, dry environment, away from direct sunlight and sources of moisture. It is recommended to keep it in a sealed container to prevent exposure to air and humidity, which can affect its stability. Due to its sensitivity to UV light, it is advisable to use amber-colored glass containers to minimize degradation. In laboratory settings, it should be handled with appropriate personal protective equipment, including gloves and safety goggles, to ensure safe handling. Proper ventilation is also essential when working with this compound to avoid inhalation of vapors. Always follow standard laboratory safety protocols to maintain a safe working environment.

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