Pentafluorobenzoyl Chloride TCI P0807

Chemical Identity

CAS No.: 2251-50-5
PubChem: CID 75256·SID 87574938
Formula: C7ClF5O
Molecular weight: 230.52 g/mol
Purity: >98.0%(GC)
Reference databases: ChEBI·ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2,3,4,5,6-pentafluorobenzoyl chloride
SMILES: C1(=C(C(=C(C(=C1F)F)F)F)F)C(=O)Cl
InChIKey: MYHOHFDYWMPGJY-UHFFFAOYSA-N

Rp 1.273.650,00

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Pentafluorobenzoyl Chloride is a chemical compound widely utilized in organic reactions, particularly in the synthesis of fluorinated compounds. As a fluorinated building block, it plays a crucial role in laboratories by enabling the creation of complex molecules with specific fluorine substitutions. Its unique molecular structure, featuring a highly reactive pentafluorobenzoil group, makes it an essential reagent in various synthetic pathways. This compound is commonly employed in nucleophilic substitution reactions and carbon activation processes, contributing to the development of advanced chemical materials and pharmaceuticals.

The reactivity and polarity of Pentafluorobenzoyl Chloride make it a preferred choice for chemists seeking precise fluorination reactions. Its ability to readily react with substrates such as amines, alcohols, and aromatic compounds ensures its versatility in different synthetic strategies. The compound’s high reactivity requires careful handling and controlled reaction conditions to achieve optimal results. These properties make it an ideal reagent for applications requiring selective fluorine substitution, particularly in research settings where precision is critical.

In Indonesian laboratories, Pentafluorobenzoyl Chloride is extensively used in organic chemistry and pharmaceutical research. It is a key component in the development of new compounds with specialized properties, supporting both academic and industrial research. Its widespread application in these fields underscores its importance as a fundamental building block in fluorinated chemistry.

Related TCI products

Organic synthesis for fluorinated compound development due to its reactive pentafluorobenzoil group.
Nucleophilic substitution reactions where selective fluorination is required for molecular modification.
Carbon activation processes to enhance the reactivity of aromatic substrates in synthetic pathways.
Pharmaceutical research for the creation of fluorinated drug molecules with improved biological activity.
Material science applications in the production of advanced fluorinated polymers and coatings.

Brand	TCI
CAS number	2251-50-5
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Fluorinated Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Liquid
Storage	Store in a cool, dry place away from light and moisture

Pentafluorobenzoyl Chloride should be stored in a cool, dry environment, away from direct light and moisture to maintain its stability. It is recommended to use airtight containers made of materials compatible with its chemical nature, such as glass or high-density polyethylene. Due to its high reactivity, it must be handled with care, using appropriate personal protective equipment like gloves and goggles. The compound should be kept in a well-ventilated area to prevent exposure to vapors. Proper labeling and storage segregation from incompatible substances are essential to ensure laboratory safety and prevent accidental reactions.

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