2,4-Bis(trifluoromethyl)benzaldehyde TCI B4206

Chemical Identity

CAS No.: 59664-42-5
PubChem: CID 2736095·SID 253660069
Formula: C9H4F6O
Molecular weight: 242.12 g/mol
Purity: >97.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2,4-bis(trifluoromethyl)benzaldehyde
SMILES: C1=CC(=C(C=C1C(F)(F)F)C(F)(F)F)C=O
InChIKey: DLRCWXOCZIUZBS-UHFFFAOYSA-N

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2,4-Bis(trifluoromethyl)benzaldehyde 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 fluorinated compounds. Its unique structure, featuring two trifluoromethyl groups and an aldehyde group, makes it a versatile reagent in synthetic chemistry. This compound is essential for researchers aiming to create new materials, pharmaceuticals, or specialty chemicals with tailored properties.

The compound's fluorinated substituents provide it with enhanced chemical stability and specific reactivity, making it a preferred choice in organic synthesis. The presence of fluorine alters the electronic properties of the molecule, influencing its reactivity in nucleophilic, condensation, and substitution reactions. These characteristics make it highly sought after in both academic and industrial research environments. Its ability to participate in a wide range of chemical transformations further solidifies its importance in modern chemical research.

In Indonesian laboratories, 2,4-Bis(trifluoromethyl)benzaldehyde is commonly used in organic chemistry research, especially in pharmaceutical and materials science applications. Researchers rely on its structural versatility to design and synthesize new compounds with specific functional properties. Its role in creating fluorinated aromatic compounds is particularly valuable for developing advanced materials and drug candidates.

TCI brochures (PDF)

Fluorination Reagents, Fluorinated Building Blocks 2026-03-18 · p. 41

Related TCI products

Organic synthesis for creating fluorinated aromatic compounds due to its reactive aldehyde group and fluorinated substituents.
Pharmaceutical research for developing new drug molecules with enhanced stability and bioavailability through fluorination.
Material science applications in the production of specialty polymers and coatings with improved chemical resistance.
Academic research in fluorinated chemistry to explore novel reaction pathways and molecular structures.
Industrial chemical development for the synthesis of intermediates used in specialty chemical manufacturing.

Brand	TCI
CAS number	59664-42-5
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Fluorinated Building Blocks
Pack sizes	Available in standard laboratory quantities as per supplier specifications
Physical form	Solid or liquid, depending on supplier packaging
Storage	Store in a cool, dry place away from moisture and direct sunlight

This compound should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which may affect its stability. Due to its fluorinated nature, it is important to handle it with appropriate personal protective equipment, including gloves and safety goggles. Avoid contact with incompatible substances such as strong oxidizers. Ensure proper ventilation in the laboratory to minimize inhalation risks. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use in research applications.

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