Ethyl 3-Fluorobenzoate TCI E0861

Chemical Identity

Other names: 3-Fluorobenzoic Acid Ethyl Ester
CAS No.: 451-02-5
PubChem: CID 67975·SID 125307815
Formula: C9H9FO2
Molecular weight: 168.17 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: ethyl 3-fluorobenzoate
SMILES: CCOC(=O)C1=CC(=CC=C1)F
InChIKey: SMMIKBXLEWTSJD-UHFFFAOYSA-N
MDL: MDL00000336

Rp 4.426.800,00

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Berat 25g

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Ethyl 3-Fluorobenzoate is a chemical compound widely used in laboratory settings for organic synthesis reactions. It serves as a key building block in the development of complex organic molecules, offering versatility in chemical reactions due to its functional groups. This compound is commonly utilized in research and development processes, particularly in the synthesis of pharmaceuticals and specialty chemicals. Its structural composition includes a fluorine atom on the benzene ring and an ethyl group attached to the carbon chain, making it a valuable reagent for chemists working on functional group transformations.

The chemical properties of Ethyl 3-Fluorobenzoate make it a preferred choice for laboratory applications. It exhibits moderate stability under controlled conditions but is sensitive to high temperatures and UV exposure. The presence of the fluorine atom contributes to its low polarity and limited solubility in organic solvents, which is advantageous in reactions requiring precise control over reaction environments. Additionally, its high reactivity allows it to participate in various types of chemical reactions, including substitution, addition, and electrophilic reactions, making it a versatile reagent in synthetic chemistry.

In Indonesian laboratories, Ethyl 3-Fluorobenzoate is frequently used in academic and industrial research settings. It is a common component in the synthesis of new compounds and is often found in chemical research labs focused on drug development and material science. Its role in creating compounds with specific functional properties makes it an essential material for researchers working on advanced chemical projects in Indonesia.

TCI brochures (PDF)

Fluorination Reagents, Fluorinated Building Blocks 2026-03-18 · p. 12

Related TCI products

Organic synthesis of pharmaceuticals and specialty chemicals due to its reactivity and functional group versatility.
Development of new compounds in material science research requiring controlled reaction environments.
Functional group transformations in academic research for the synthesis of complex organic molecules.
Chemical reactions involving substitution, addition, and electrophilic mechanisms in synthetic chemistry.
Research in drug development where precise chemical structures are essential for biological activity.

Brand	TCI
CAS number	451-02-5
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Fluorinated Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid or liquid, depending on the specific product variant
Storage	Store in a cool, dark place away from heat and UV light

Ethyl 3-Fluorobenzoate should be stored in a cool, dark environment to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to moisture and air, which can affect its reactivity. Due to its sensitivity to high temperatures and UV light, it should be kept away from direct sunlight and heat sources. In laboratory settings, proper ventilation is essential to ensure safe handling. Always use appropriate personal protective equipment when working with this compound to minimize exposure risks. The compound should be stored in a designated chemical storage area that complies with safety regulations to ensure the safety of laboratory personnel and the integrity of the material.

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