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56609-83-7

4-SEC-BUTYLBENZENESULFONYL CHLORIDE

Catalog#: AR00EEVA  |   CAS#: 56609-83-7  |   MDL#: MFCD00024886  |   MF: C10H13ClO2S  |   MW: 232.7270

Packsize Purity Price Availability Quantity
250mg 95% $52.00 2-3 weeks Buy Now Add To Cart
500mg 95% $58.00 2-3 weeks Buy Now Add To Cart
1g 95% $67.00 2-3 weeks Buy Now Add To Cart
2.5g 95% $113.00 2-3 weeks Buy Now Add To Cart
5g 95% $190.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR00EEVA
Chemical Name 4-SEC-BUTYLBENZENESULFONYL CHLORIDE
CAS Number 56609-83-7
Molecular Formula C10H13ClO2S
Molecular Weight 232.7270
MDL Number MFCD00024886
SMILES CCC(c1ccc(cc1)S(=O)(=O)Cl)C

4-(sec-Butyl)benzene-1-sulfonyl chloride, also known as sec-Butylbenzenesulfonyl chloride, is a versatile chemical reagent commonly used in organic synthesis. It serves as a sulfonylating agent, introducing the sulfonyl group (-SO2Cl) onto various functional groups in organic molecules. This compound is widely employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials due to its ability to modify the reactivity and properties of target compounds.One key application of 4-(sec-Butyl)benzene-1-sulfonyl chloride is in the protection and activation of hydroxyl (-OH) groups in alcohol-containing molecules. By selectively reacting with the hydroxyl groups, this reagent forms sulfonyl esters, which can serve as temporary protecting groups for alcohols during multi-step synthesis processes. Upon completion of the desired reactions, the sulfonyl group can be easily removed to regenerate the original alcohol functionality.Furthermore, 4-(sec-Butyl)benzene-1-sulfonyl chloride is utilized in the preparation of sulfonamides, a class of compounds with diverse applications in medicinal chemistry. The sulfonyl chloride group can react with amines to form sulfonamide linkages, which are prevalent in pharmaceuticals and biologically active molecules. This transformation enables the introduction of sulfonamide moieties into target molecules, imparting specific pharmacological properties or enhancing their biological activity.In summary, the strategic use of 4-(sec-Butyl)benzene-1-sulfonyl chloride in chemical synthesis allows for precise modification of functional groups, enabling the synthesis of complex molecules with tailored properties for various applications in the field of organic chemistry and drug discovery.
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