2-Methanesulfonamido-3-methylbenzoic acid, identified by its CAS number 926206-21-5, is an organic compound that features a benzoic acid structure with a methyl group and a methanesulfonamide functional group. This compound is characterized by its sulfonamide moiety, which typically enhances solubility in polar solvents and can influence biological activity. The presence of the methyl group on the benzene ring can affect the compound's steric and electronic properties, potentially impacting its reactivity and interactions with biological targets. As a benzoic acid derivative, it may exhibit acidic properties, allowing it to participate in acid-base reactions. Additionally, the methanesulfonamide group can contribute to hydrogen bonding capabilities, which may enhance its interactions in various chemical environments. This compound may be of interest in pharmaceutical research due to its potential biological activities, including antimicrobial or anti-inflammatory properties, although specific biological data would need to be referenced for detailed applications. Overall, its unique structure suggests a range of potential uses in medicinal chemistry and related fields.

2-MethanesulfonaMido-3-Methylbenzoic acid

926206-21-5: 2-Methanesulfonamido-3-methylbenzoic acid, identified by its CAS number 926206-21-5, is an organic compound that features a benzoic acid structure with a methyl group and a methanesulfonamide functional group. This compound is characterized by its sulfonamide moiety, which typically enhances solubility in polar solvents and can influence biological activity. The presence of the methyl group on the benzene ring can affect the compound's steric and electronic properties, potentially impacting its reactivity and interactions with biological targets. As a benzoic acid derivative, it may exhibit acidic properties, allowing it to participate in acid-base reactions. Additionally, the methanesulfonamide group can contribute to hydrogen bonding capabilities, which may enhance its interactions in various chemical environments. This compound may be of interest in pharmaceutical research due to its potential biological activities, including antimicrobial or anti-inflammatory properties, although specific biological data would need to be referenced for detailed applications. Overall, its unique structure suggests a range of potential uses in medicinal chemistry and related fields.

2-(methanesulfonamido)-3-methylbenzoic acid

<p>3-Methyl-2-(methylsulfonamido)benzoic acid</p>

CAS 926206-21-5

2-MethanesulfonaMido-3-Methylbenzoic acid

2-(methanesulfonamido)-3-methylbenzoic acid

Ref: IN-DA00IH8N

3-Methyl-2-(methylsulfonamido)benzoic acid

Ref: 54-OR470318

3-Methyl-2-(methylsulfonamido)benzoic acid

Ref: 10-F626494