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CAS 37073-18-0

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N-(2-aminophenyl)methanesulfonamide

Description:
N-(2-aminophenyl)methanesulfonamide, also known as a sulfonamide compound, is characterized by its sulfonamide functional group (-SO2NH2) attached to a phenyl ring that has an amino group (-NH2) in the ortho position. This compound typically exhibits properties such as being a solid at room temperature, with potential solubility in polar solvents due to the presence of both the sulfonamide and amino groups, which can engage in hydrogen bonding. It may display moderate stability under standard conditions but can be sensitive to heat and moisture. The presence of the amino group suggests potential for biological activity, as many sulfonamides are known for their antibacterial properties. Additionally, the compound may participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it of interest in medicinal chemistry and drug development. Its specific applications and reactivity can vary based on the surrounding chemical environment and the presence of other functional groups.
Formula:C7H10N2O2S
InChI:InChI=1/C7H10N2O2S/c1-12(10,11)9-7-5-3-2-4-6(7)8/h2-5,9H,8H2,1H3
SMILES:CS(=O)(=O)Nc1ccccc1N
Synonyms:
  • Methanesulfonamide, N-(2-aminophenyl)-
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