2-Fluoro-4-nitroanisole TCI F0617

Chemical Identity

Other names: 2-Fluoro-1-methoxy-4-nitrobenzene
CAS No.: 455-93-6
PubChem: CID 223104·SID 87559602
Formula: C7H6FNO3
Molecular weight: 171.13 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-fluoro-1-methoxy-4-nitrobenzene
SMILES: COC1=C(C=C(C=C1)[N+](=O)[O-])F
InChIKey: XGMVTXUXZUPGGY-UHFFFAOYSA-N
MDL: MDL00061095

Rp 452.550,00

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2-Fluoro-4-nitroanisole is a chemical compound widely used as a building block in the synthesis of complex organic molecules. Its aromatic structure, combined with fluorine and nitro substituents, makes it a versatile reagent in various chemical reactions. This compound is commonly employed in organic chemistry laboratories for its ability to participate in nitration, fluorination, and electrophilic substitution reactions. Its unique chemical profile allows researchers to create derivatives with specific biological or chemical properties, making it a valuable tool in synthetic chemistry.

The compound’s stable chemical structure and controlled reactivity make it a preferred choice for laboratory applications. It exhibits good solubility in organic solvents, which simplifies processing and isolation steps in synthesis protocols. Additionally, its predictable behavior under different reaction conditions ensures reliable results, enhancing its utility in both academic and industrial research settings. These properties contribute to its widespread use in the development of new compounds with potential pharmaceutical or industrial applications.

In Indonesian laboratories, 2-Fluoro-4-nitroanisole is frequently used in organic chemistry research, particularly in the synthesis of bioactive compounds and functionalized aromatic derivatives. Its availability in various packaging options supports both small-scale and larger research projects. Researchers in Indonesia rely on this compound for its reliability and effectiveness in creating complex molecular structures with specific functional groups.

TCI brochures (PDF)

Fluorination Reagents, Fluorinated Building Blocks 2026-03-18 · p. 22

Related TCI products

Organic synthesis of bioactive compounds due to its aromatic structure and reactive substituents.
Nitration reactions where nitro groups are essential for functional group introduction.
Fluorination processes to introduce fluorine atoms for enhanced molecular properties.
Electrophilic substitution reactions to modify aromatic rings with specific substituents.
Structural modification studies to explore reactivity and stability of aromatic compounds.

Brand	TCI
CAS number	455-93-6
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Fluorinated Building Blocks
Pack sizes	Available in various sizes to suit different laboratory needs
Physical form	Solid
Storage	Store in a cool, dry place away from light and moisture

2-Fluoro-4-nitroanisole should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent exposure to air and humidity. Due to its potential reactivity, it should be handled in a well-ventilated area, ideally with appropriate personal protective equipment. Avoid contact with incompatible substances such as strong acids or bases. Proper labeling and storage conditions are essential to ensure safety and maintain the integrity of the compound during laboratory use.

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