5-Fluoro-2-nitrobenzaldehyde TCI F0645

Chemical Identity

CAS No.: 395-81-3
PubChem: CID 587090·SID 87559848
Formula: C7H4FNO3
Molecular weight: 169.11 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 5-fluoro-2-nitrobenzaldehyde
SMILES: C1=CC(=C(C=C1F)C=O)[N+](=O)[O-]
InChIKey: KKAFVHUJZPVWND-UHFFFAOYSA-N
MDL: MDL00153175

Rp 955.500,00

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5-Fluoro-2-nitrobenzaldehyde is a versatile organic compound widely used in laboratory settings for the synthesis of complex molecules. It serves as a key building block in chemical reactions due to its functional aldehyde group and the presence of both fluorine and nitro substituents. These groups contribute to its unique reactivity and electronic properties, making it a valuable tool in synthetic chemistry. Its role in laboratory research is critical, especially in the development of pharmaceutical compounds and bioactive molecules.

This compound is preferred for its ability to participate in various chemical reactions, including reduction, substitution, and nucleophilic attacks. The combination of a fluorine atom and a nitro group imparts specific electronic characteristics that allow it to act as either an electron donor or acceptor, depending on the reaction conditions. This versatility enables chemists to tailor reactions with high precision, making it a favored choice in advanced synthetic pathways.

In Indonesian laboratories, 5-Fluoro-2-nitrobenzaldehyde is commonly used in organic chemistry research, particularly in pharmaceutical and bioactive compound synthesis. It is a staple in academic and industrial research settings where the synthesis of complex molecules requires precise control over reactivity and molecular structure. Its application is widespread across various scientific disciplines, supporting innovation in chemical research and development.

TCI brochures (PDF)

Fluorination Reagents, Fluorinated Building Blocks 2026-03-18 · p. 25

Related TCI products

Organic synthesis of pharmaceutical compounds due to its reactivity and structural versatility.
Development of bioactive molecules through controlled chemical reactions and functional group manipulation.
Research in heterocyclic chemistry where electron-donating and accepting properties are essential.
Synthesis of aromatic derivatives for use in medicinal chemistry and drug discovery.
Investigation of electrophilic and nucleophilic reactions in advanced chemical processes.

Brand	TCI
CAS number	395-81-3
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Fluorinated Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid or liquid, depending on supplier packaging
Storage	Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment, away from direct sunlight and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its sensitivity to oxidation and hydrolysis, it should be handled with care to avoid degradation. Proper personal protective equipment, such as gloves and safety goggles, should be worn when handling. It is important to ensure that storage conditions are stable to maintain the compound's chemical integrity and effectiveness in laboratory applications.

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