AA16345
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.
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 |
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.