Methyl (4-Fluorobenzoyl)acetate TCI F0472

Chemical Identity

Other names: (4-Fluorobenzoyl)acetic Acid Methyl Ester · Methyl 3-(4-Fluorophenyl)-3-oxopropionate · 3-(4-Fluorophenyl)-3-oxopropionic Acid Methyl Ester
CAS No.: 63131-29-3
PubChem: CID 579425·SID 87570228
Formula: C10H9FO3
Molecular weight: 196.18 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: methyl 3-(4-fluorophenyl)-3-oxopropanoate
SMILES: COC(=O)CC(=O)C1=CC=C(C=C1)F
InChIKey: HGLVYXXPRSNKQN-UHFFFAOYSA-N
MDL: MDL00000355

Rp 717.150,00

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Methyl (4-Fluorobenzoyl)acetate is a chemical compound widely used in organic reactions for the synthesis of complex molecules. As a fluorinated building block, it serves as a fundamental component in the creation of compounds with specific structural features. This reagent is particularly valuable in laboratory settings where precise chemical transformations are required. Its versatility makes it an essential tool for chemists working on a variety of synthetic pathways.

The compound is known for its stable molecular structure and moderate reactivity, which contribute to its effectiveness in various synthetic applications. It is non-volatile and dissolves readily in organic solvents, simplifying its handling and integration into chemical processes. These properties make it a preferred choice for laboratory use, especially in reactions involving esterification or substitution. Its reliability and consistency ensure reproducible results, which are crucial in research environments.

In Indonesian laboratories, Methyl (4-Fluorobenzoyl)acetate is commonly used in organic chemistry research, particularly in the development of new compounds with pharmaceutical or industrial applications. It is also frequently employed in studies involving fluorinated compounds, which have potential in medical and materials science fields. Its role in advancing chemical research is well recognized among scientists and researchers in the region.

Related TCI products

Organic synthesis of fluorinated compounds due to its stable structure and reactivity.
Esterification reactions where a fluoro group and a carbonyl group are required.
Substitution reactions in the development of pharmaceutical intermediates.
Research on fluorinated materials for advanced material science applications.
Investigation of bioactive compounds with potential pharmaceutical properties.

Brand	TCI
CAS number	63131-29-3
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Fluorinated Building Blocks
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Liquid
Storage	Store in a cool, dry place away from direct sunlight

Methyl (4-Fluorobenzoyl)acetate should be stored in a cool, dry place, away from direct sunlight and heat sources. It is recommended to use airtight containers made of glass or polyethylene to prevent contamination and maintain purity. Since it is non-volatile, it does not require special refrigeration, but it should be kept in a secure location to avoid accidental spills. In laboratory settings, it is important to handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Proper ventilation should be ensured when working with this reagent to minimize exposure. Its stable nature makes it suitable for long-term storage, provided it is kept under the recommended conditions.

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