Pentafluorophenyl Benzoate TCI P2229

Chemical Identity

CAS No.: 1548-84-1
Formula: C13H5F5O2
Molecular weight: 288.17 g/mol
Purity: >98.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2,3,4,5,6-pentafluorophenyl) benzoate
SMILES: C1=CC=C(C=C1)C(=O)OC2=C(C(=C(C(=C2F)F)F)F)F
InChIKey: WZPWTXZSQHIABL-UHFFFAOYSA-N
PubChem: CID 11011649

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Pentafluorophenyl Benzoate is a chemical compound widely used in organic synthesis as a building block for creating complex molecular structures. This compound features a benzoate group attached to a pentafluorophenyl group, which imparts unique reactivity and functional versatility. In laboratory settings, it serves as a key reagent in various synthetic pathways, including substitution reactions and Friedel-Crafts reactions. Its ability to participate in fluorination processes makes it an essential tool for researchers working on fluorinated compounds.

The compound’s chemical stability under controlled conditions, combined with its high reactivity towards organic reagents, makes it a preferred choice for synthetic chemists. Its solubility in organic solvents simplifies purification and isolation steps, enhancing the efficiency of laboratory workflows. The presence of fluorine atoms in its structure also contributes to its utility in creating compounds with specific physical and chemical properties. These characteristics make it a valuable reagent in both academic and industrial research environments.

In Indonesian laboratories, Pentafluorophenyl Benzoate is commonly used in organic chemistry research, particularly in higher education institutions and research organizations. Its reactivity and functional versatility make it a go-to compound for studies involving fluorinated molecules. It is frequently applied in the development of new materials, pharmaceuticals, and specialty chemicals, supporting a wide range of scientific investigations.

Organic synthesis for creating fluorinated compounds due to its reactivity and functional versatility.
Friedel-Crafts reactions where it acts as a key reagent for aromatic substitution processes.
Fluorination studies as it readily forms fluorinated derivatives with various functional groups.
Research in pharmaceutical development for synthesizing bioactive molecules with fluorine atoms.
Material science applications for producing advanced polymers and specialty chemical products.

Brand	TCI
CAS number	1548-84-1
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Fluorinated Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid or liquid depending on formulation
Storage	—

Pentafluorophenyl Benzoate should be stored in a cool, dry place away from direct sunlight and sources of heat. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled in a well-ventilated area, ideally with proper personal protective equipment. Avoid contact with incompatible substances such as strong bases or reducing agents. Storage conditions should maintain stability and ensure safety during handling and use in laboratory environments.

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