Pentafluorophenyl Acetate TCI P2192

Chemical Identity

CAS No.: 19220-93-0
Formula: C8H3F5O2
Molecular weight: 226.10 g/mol
Purity: >98.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2,3,4,5,6-pentafluorophenyl) acetate
SMILES: CC(=O)OC1=C(C(=C(C(=C1F)F)F)F)F
InChIKey: ZXTVBLZVILLKPM-UHFFFAOYSA-N
PubChem: CID 87968

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Pentafluorophenyl Acetate is a chemical compound widely used in organic synthesis reactions within laboratory settings. It is a key reagent in the field of protection, deprotection, and derivatization, playing a crucial role in the synthesis of complex organic molecules. The compound consists of a pentafluorophenyl group attached to an acetyl group, which makes it highly reactive and suitable for specific chemical transformations. Its unique structure allows it to participate in various functional group manipulations, making it an essential tool for chemists working on intricate molecular designs.

The chemical stability and controlled reactivity of Pentafluorophenyl Acetate make it a preferred choice in laboratory applications. The pentafluorophenyl group imparts strong electron-withdrawing properties, enabling selective reactions and enhancing the efficiency of deprotection processes. This compound is known for its high solubility in organic solvents such as ethyl acetate and chloroform, which facilitates its use in a wide range of synthetic procedures. Its reliability and consistency in performance contribute to its popularity among researchers.

In Indonesian laboratories, Pentafluorophenyl Acetate is commonly used in research focused on organic chemistry, particularly in the development of pharmaceuticals and fine chemicals. Its role in deprotection and derivatization is vital for the synthesis of compounds requiring precise functional group control. The compound is also employed in analytical chemistry for sample preparation and derivatization techniques. Its availability and performance make it a valuable resource for academic and industrial research in Indonesia.

Organic synthesis reactions where selective deprotection and derivatization are required.
Preparation of complex organic molecules with controlled functional group reactivity.
Analytical chemistry applications involving sample derivatization for enhanced detection.
Pharmaceutical research for the development of new drug compounds through functional group manipulation.
Chemical research focused on the study of reactivity and stability of pentafluorophenyl groups.

Brand	TCI
CAS number	19220-93-0
Molecular formula	—
Purity	—
Category	Chemistry > Synthetic Reagents > Protection, Deprotection, Derivatization
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid or liquid depending on the specific product formulation
Storage	Store in a cool, dry place away from moisture and direct sunlight

Pentafluorophenyl Acetate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in airtight containers to prevent exposure to moisture and air, which may affect its reactivity. Proper labeling of storage containers is essential for safety and identification. In laboratory settings, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. Due to its chemical nature, it should be stored away from incompatible materials such as strong bases or reactive metals. Regular monitoring of storage conditions ensures the compound remains effective for its intended applications.

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