N-(2-formylphenyl)methanesulfonamide is an organic compound characterized by the presence of a sulfonamide functional group attached to a phenyl ring that bears a formyl substituent. This compound features a methanesulfonamide moiety, which contributes to its potential as a sulfonamide derivative. The formyl group indicates the presence of an aldehyde functional group, which can participate in various chemical reactions, including condensation and oxidation. The compound is likely to exhibit polar characteristics due to the sulfonamide and aldehyde groups, influencing its solubility in polar solvents. Additionally, the presence of the aromatic ring may impart stability and influence the compound's reactivity. N-(2-formylphenyl)methanesulfonamide may have applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the biological activity often associated with sulfonamide compounds. Its specific properties, such as melting point, boiling point, and reactivity, would require empirical measurement or detailed literature references for precise characterization.

N-(2-formylphenyl)methanesulfonamide

94532-99-7: Methanesulfonamide, N-(2-formylphenyl)-,  N-(2-Formylphenyl)methanesulfonamide

2-(Methylsulfonamido)benzaldehyde

_x005F_x000D_2-(Methylsulfonamido)benzaldehyde

The Wittig reaction is a type of chemical reaction that involves the conversion of an alkyl halide to an alkene using a phosphine and a compound containing a double bond. The reaction is usually conducted in the presence of an acid catalyst, such as sulfuric acid or hydrochloric acid. The reaction proceeds by addition of the phosphine to the halide followed by nucleophilic attack on the carbonyl carbon. This leads to formation of a new carbon-carbon bond and release of phosphorus as inorganic phosphate.

The kinetic experimentally determined that when 2-(methylsulfonamido)benzaldehyde was reacted with γ-aminobutyric acid (GABA), it yielded 2-(methylsulfonamido)benzoic acid with an efficiency of 51%. The yield for this experiment was calculated by taking the weight percent change in reactants minus the weight percent change in products and then dividing that number by 100. 

2-(

CAS 94532-99-7: N-(2-formylphenyl)methanesulfonamide

2-(Methylsulfonamido)benzaldehyde

Ref: 54-OR965391

_x005F_x000D_2-(Methylsulfonamido)benzaldehyde

Ref: IN-DA003F31

2-(Methylsulfonamido)benzaldehyde

Ref: 10-F377750

2-(Methylsulfonamido)benzaldehyde

Ref: 3D-UDA53299