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1146290-36-9

Benzenesulfonyl chloride, 2-fluoro-4-nitro-

Catalog#: AR000FKO  |   CAS#: 1146290-36-9  |   MDL#: MFCD11858095  |   MF: C6H3ClFNO4S  |   MW: 239.6087

Packsize Purity Price Availability Quantity
50mg 97% $6.00 Global Stock Buy Now Add To Cart
100mg 97% $8.00 Global Stock Buy Now Add To Cart
250mg 97% $18.00 Global Stock Buy Now Add To Cart
1g 97% $54.00 Global Stock Buy Now Add To Cart
5g 97% $257.00 Global Stock Buy Now Add To Cart
10g 97% $481.00 Global Stock Buy Now Add To Cart
25g 97% $1,068.00 Global Stock Buy Now Add To Cart
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Catalog Number AR000FKO
Chemical Name Benzenesulfonyl chloride, 2-fluoro-4-nitro-
CAS Number 1146290-36-9
Molecular Formula C6H3ClFNO4S
Molecular Weight 239.6087
MDL Number MFCD11858095
SMILES Fc1cc(ccc1S(=O)(=O)Cl)[N+](=O)[O-]

2-Fluoro-4-nitrobenzene-1-sulfonyl chloride is a versatile chemical reagent commonly used in organic synthesis. This compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique chemical structure makes it a valuable intermediate in the synthesis of complex organic compounds.In chemical synthesis, 2-Fluoro-4-nitrobenzene-1-sulfonyl chloride can be utilized as a sulfonylating agent, allowing for the introduction of the sulfonyl functional group into organic molecules. This reaction is particularly useful in medicinal chemistry and drug development, where the presence of the sulfonyl group can enhance the biological activity and pharmacokinetic properties of the final compound.Furthermore, the reactivity of 2-Fluoro-4-nitrobenzene-1-sulfonyl chloride allows for the selective modification of aromatic compounds, enabling chemists to exert precise control over the functionalization of target molecules. This level of control is essential in the design and synthesis of novel materials and compounds with tailored properties for specific applications in various industries.Overall, the strategic incorporation of 2-Fluoro-4-nitrobenzene-1-sulfonyl chloride in chemical synthesis enables chemists to access a wide range of structurally diverse and complex molecules, making it a valuable tool in the field of organic chemistry.
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