logo
Home  > N-(2-Iodophenyl)methanesulfonamide

AA16345

116547-92-3 | N-(2-Iodophenyl)methanesulfonamide

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $413.00 $289.00 -   +
1g 95% in stock $792.00 $554.00 -   +
5g 95% in stock $2,302.00 $1,611.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA16345
Chemical Name: N-(2-Iodophenyl)methanesulfonamide
CAS Number: 116547-92-3
Molecular Formula: C7H8INO2S
Molecular Weight: 297.1134
MDL Number: MFCD00978524
SMILES: Ic1ccccc1NS(=O)(=O)C

 

Upstream Synthesis Route
  • Methanesulfonamide, N-(2-iodophenyl)- is a versatile compound widely used in chemical synthesis as a powerful nucleophilic reagent. Its unique structure allows it to participate in a variety of synthetic reactions, making it a valuable tool for organic chemists.One key application of Methanesulfonamide, N-(2-iodophenyl)- is in the formation of C-C and C-N bonds through nucleophilic substitution reactions. By serving as a nucleophile, this compound can react with various electrophiles, such as alkyl halides or acyl chlorides, to introduce the 2-iodophenyl group into the target molecule. This ability to functionalize organic compounds at specific positions is essential in the synthesis of complex molecules for pharmaceuticals, agrochemicals, and materials science.Furthermore, Methanesulfonamide, N-(2-iodophenyl)- can also be utilized in transition metal-catalyzed cross-coupling reactions. In these reactions, the 2-iodophenyl group acts as a leaving group that undergoes coupling with another organometallic reagent, leading to the formation of new carbon-carbon or carbon-heteroatom bonds. This methodology enables the construction of biaryl compounds and other structurally diverse molecules with high efficiency and selectivity.Overall, Methanesulfonamide, N-(2-iodophenyl)- plays a crucial role in modern organic synthesis by facilitating the construction of complex molecular architectures through efficient and selective bond-forming reactions. Its versatility and reactivity make it a valuable reagent for chemists working in various fields of chemical research and development.
FEATURED PRODUCTS