4-Fluorobenzophenone is a chemical compound widely used as a building block in various organic reactions. It consists of a benzophenone ring with a fluorine atom attached at the fourth position. This compound plays a crucial role in laboratory settings, particularly in the synthesis of complex molecules. Its structural simplicity and functional versatility make it an essential component in organic chemistry and pharmaceutical research. Due to its stability and controlled reactivity, it is frequently employed in substitution and coupling reactions, contributing to the development of new compounds with specific functionalities.
The compound's chemical properties, including high polarity and electronegativity due to the fluorine group, make it a preferred choice for synthetic chemists. These characteristics allow for effective participation in various reaction mechanisms. Its stability under normal conditions ensures that it remains chemically inert until exposed to specific reagents such as strong bases, acids, or organic solvents. This controlled reactivity is vital for achieving desired outcomes in complex synthetic pathways without unintended side reactions.
In Indonesian laboratories, 4-Fluorobenzophenone is commonly used in organic chemistry, pharmaceutical, and material research. It is an important reagent in the development of new compounds with specific structural and functional properties. Its availability and reliability make it a key material for researchers aiming to explore new chemical syntheses and applications.
TCI brochures (PDF)
- Fluorination Reagents, Fluorinated Building Blocks 2026-03-18 · p. 14
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- Organic synthesis: This compound is ideal for creating complex molecules due to its reactivity and structural versatility.
- Pharmaceutical research: It is used in the development of new drugs, as its fluorinated group can influence biological activity.
- Material science: It contributes to the synthesis of advanced materials with specific chemical and physical properties.
- Coupling reactions: Its stability and controlled reactivity make it suitable for efficient coupling processes in synthetic chemistry.
- Functional group modification: The fluorine group allows for targeted modifications, enhancing the compound's utility in synthetic pathways.
| Brand | TCI |
|---|---|
| CAS number | 345-83-5 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Building Blocks > Fluorinated Building Blocks |
| Pack sizes | Available in various quantities as per standard laboratory supply |
| Physical form | Solid |
| Storage | Store in a cool, dry place away from moisture and direct sunlight |
4-Fluorobenzophenone should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a tightly sealed container to prevent exposure to moisture and air. Due to its reactivity with strong acids and bases, it should be handled in a well-ventilated area with appropriate personal protective equipment. Avoid contact with incompatible materials to ensure safe laboratory practices. Regular inspection of storage conditions is advised to maintain the integrity of the compound. Proper labeling and storage practices are essential to prevent accidental exposure and ensure safe handling in the laboratory.
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