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6668-56-0

4-FLUORO-3-NITROBENZENESULFONYL CHLORIDE

Catalog#: AR00FDYG  |   CAS#: 6668-56-0  |   MDL#: MFCD06342770  |   MF: C6H3ClFNO4S  |   MW: 239.6087

Packsize Purity Price Availability Quantity
100mg 95% $10.00 Global Stock Buy Now Add To Cart
250mg 95% $13.00 Global Stock Buy Now Add To Cart
1g 95% $24.00 Global Stock Buy Now Add To Cart
5g 95% $77.00 Global Stock Buy Now Add To Cart
10g 95% $142.00 Global Stock Buy Now Add To Cart
25g 95% $322.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00FDYG
Chemical Name 4-FLUORO-3-NITROBENZENESULFONYL CHLORIDE
CAS Number 6668-56-0
Molecular Formula C6H3ClFNO4S
Molecular Weight 239.6087
MDL Number MFCD06342770
SMILES [O-][N+](=O)c1cc(ccc1F)S(=O)(=O)Cl

4-Fluoro-3-nitrobenzenesulfonyl chloride is a versatile compound widely utilized in chemical synthesis for its unique reactivity and functional group compatibility. As a sulfonyl chloride derivative, this compound serves as a valuable building block in the synthesis of various pharmaceuticals, agrochemicals, and advanced materials.One of the key applications of 4-Fluoro-3-nitrobenzenesulfonyl chloride is as a sulfonylating agent in organic reactions. Its sulfonyl chloride group is highly reactive towards nucleophiles, allowing for facile introduction of sulfonyl functionalities into organic molecules. This reactivity makes it an important reagent in the preparation of sulfonamides, sulfonates, and other sulfur-containing compounds.Additionally, 4-Fluoro-3-nitrobenzenesulfonyl chloride can serve as a protecting group for amines and alcohols in organic synthesis. By selectively blocking the reactive sites of these functional groups with the sulfonyl chloride moiety, chemists can perform elaborate multi-step synthetic sequences with improved selectivity and efficiency.Furthermore, this compound is a valuable intermediate in the preparation of complex pharmaceutical compounds, where the sulfonyl chloride functionality can be selectively transformed into other functional groups through a series of well-defined chemical transformations. Its presence in the molecular structure imparts desirable physicochemical properties and biological activities to the final product.Overall, 4-Fluoro-3-nitrobenzenesulfonyl chloride plays a crucial role in modern chemical synthesis by enabling the efficient construction of diverse chemical structures with specific functionalities, making it an indispensable tool for synthetic chemists in academia and industry.
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