4-Fluorobenzenesulfonyl Chloride is a chemical compound widely used as a building block in the synthesis of complex organic compounds. It contains both a fluorine group and a sulfonyl chloride functional group, making it a versatile reagent in organic chemistry. This compound plays a crucial role in various laboratory processes, particularly in reactions involving substitution and bond formation. Its unique molecular structure allows it to participate in multiple chemical transformations, making it a valuable tool for researchers.
The compound's high reactivity and ability to form stable bonds with other molecules make it a preferred choice in laboratory settings. The presence of the fluorine group contributes to its stability and selectivity in reactions, reducing the likelihood of unwanted side reactions. Its chemical properties enable it to be used in a variety of synthetic pathways, including sulfonation, substitution, and condensation reactions. These characteristics enhance its utility in both academic and industrial research environments.
In Indonesian laboratories, 4-Fluorobenzenesulfonyl Chloride is commonly used in scientific research and chemical product development. It is a key component in experiments requiring fluorinated structures, supporting advancements in organic chemistry and pharmaceutical research. Its availability and consistent quality contribute to the efficiency and accuracy of laboratory work, making it an essential material for researchers in Indonesia.
TCI brochures (PDF)
- Fluorination Reagents, Fluorinated Building Blocks 2026-03-18 · p. 14
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- Organic synthesis applications benefit from its reactivity and ability to form new bonds, making it ideal for complex molecule construction.
- Pharmaceutical research utilizes this compound for developing drugs with specific fluorinated structures, enhancing drug efficacy and stability.
- Fluorination studies rely on its unique molecular structure to explore the effects of fluorine substitution in organic compounds.
- Sulfonation processes use its sulfonyl chloride group to introduce sulfonic acid functionalities into target molecules.
- Condensation reactions benefit from its ability to participate in bond-forming mechanisms, supporting the creation of diverse chemical structures.
| Brand | TCI |
|---|---|
| CAS number | 349-88-2 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Building Blocks > Fluorinated Building Blocks |
| Pack sizes | Available in standard laboratory quantities |
| Physical form | Solid |
| Storage | Store in a cool, dry place away from moisture and light |
This compound should be stored in a cool, dry environment, away from moisture and direct sunlight to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity, which could lead to degradation. Due to its reactivity, it should be handled in a well-ventilated area, ideally with appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with incompatible materials, including strong bases and reducing agents. Proper labeling and storage conditions ensure the safety of laboratory personnel and the effectiveness of the compound in experimental processes.
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