9-Anthracenecarboxaldehyde TCI A0779

Chemical Identity

CAS No.: 642-31-9
PubChem: CID 69504·SID 87562312
Formula: C15H10O
Molecular weight: 206.24 g/mol
Purity: >99.0%(GC)
Reference databases: ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: anthracene-9-carbaldehyde
SMILES: C1=CC=C2C(=C1)C=C3C=CC=CC3=C2C=O
InChIKey: YMNKUHIVVMFOFO-UHFFFAOYSA-N

Rp 1.326.150,00

~~Rp 927.150,00~~ Rp 1.326.150,00

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9-Anthracenecarboxaldehyde is a chemical compound widely used in organic reactions for the synthesis of complex molecules. It serves as a key building block in laboratory settings, particularly in the development of heterocyclic compounds and intricate molecular structures. Its aromatic structure provides stability, while its reactivity makes it a valuable tool for chemists. This compound is commonly utilized in research involving aldehyde functionalities, where its ability to participate in various reaction mechanisms is essential.

The compound's chemical properties make it a preferred choice for synthetic chemists. It exhibits high reactivity, enabling it to engage in condensation, substitution, and redox reactions. Its molecular complexity also contributes to its stability under certain conditions, making it reliable for experimental use. These characteristics ensure that it remains a staple in organic synthesis, supporting the creation of a wide range of chemical products.

In Indonesian laboratories, 9-Anthracenecarboxaldehyde is extensively used in organic chemistry research. It is commonly found in university and research institution settings, where it supports the development of new chemical compounds. Its availability and consistent quality make it a trusted material for scientific experiments and academic research. Its role in synthetic processes is crucial, especially for those requiring aldehyde-based reactivity.

TCI brochures (PDF)

Building Blocks for Organic Semiconductor 2026-03-24 · p. 9

Related TCI products

Organic synthesis of heterocyclic compounds due to its reactivity and aromatic structure.
Condensation reactions where aldehyde functionality is essential for forming complex molecules.
Redox reactions that require a stable and reactive starting material with aromatic properties.
Substitution reactions in the development of new chemical structures and functional groups.
Research applications in Indonesian universities and research institutes for academic and industrial chemistry projects.

Brand	TCI
CAS number	642-31-9
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid
Storage	Store in a cool, dry place away from light and moisture

9-Anthracenecarboxaldehyde should be stored in a cool, dry place away from direct light and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that it is kept in a well-ventilated area to minimize any potential risks. Proper storage conditions help maintain its chemical stability and ensure its effectiveness in laboratory applications. Always follow standard laboratory safety protocols when handling this compound.

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