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50702-39-1

3-Iodobenzenesulfonamide

Catalog#: AR00DZMS  |   CAS#: 50702-39-1  |   MDL#: MFCD06409088  |   MF: C6H6INO2S  |   MW: 283.0868

Packsize Purity Price Availability Quantity
50mg 95% $211.00 2-3 weeks Buy Now Add To Cart
100mg 95% $303.00 2-3 weeks Buy Now Add To Cart
250mg 95% $423.00 2-3 weeks Buy Now Add To Cart
500mg 95% $685.00 2-3 weeks Buy Now Add To Cart
1g 95% $870.00 2-3 weeks Buy Now Add To Cart
2.5g 95% $1,678.00 2-3 weeks Buy Now Add To Cart
5g 95% $2,472.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR00DZMS
Chemical Name 3-Iodobenzenesulfonamide
CAS Number 50702-39-1
Molecular Formula C6H6INO2S
Molecular Weight 283.0868
MDL Number MFCD06409088
SMILES Ic1cccc(c1)S(=O)(=O)N

3-Iodobenzenesulfonamide is a versatile compound widely utilized in chemical synthesis as a key building block in various organic reactions. Its unique molecular structure, consisting of a sulfonamide group attached to an iodobenzene ring, offers distinct reactivity and functionality that make it valuable in the creation of complex molecules.One notable application of 3-Iodobenzenesulfonamide is in the synthesis of sulfonamides, which are important pharmaceutical compounds with diverse biological activities. By utilizing this compound as a starting material, chemists can introduce the sulfonamide functionality into target molecules, thereby modulating their pharmacological properties.Additionally, 3-Iodobenzenesulfonamide is commonly employed in transition metal-catalyzed cross-coupling reactions to form C–N bonds. This type of reaction enables the efficient construction of biaryl compounds, which are prevalent in medicinal chemistry and materials science. The iodine atom in 3-Iodobenzenesulfonamide serves as a handle for further functionalization, allowing for the introduction of various substituents and the synthesis of diverse chemical structures.Furthermore, 3-Iodobenzenesulfonamide can participate in electrophilic aromatic substitution reactions, expanding its utility in the synthesis of aryl sulfonamides and related compounds. Its ability to undergo multiple modes of reactivity makes it a valuable reagent for chemists seeking to access novel molecules for biological evaluation or material design.
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GHS Pictogram N/A
UN# -
Hazard Statements -
Class -
Packing Group -

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