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CAS 51123-09-2

:

5-Amino-N-ethyl-2-methyl-N-phenylbenzenesulfonamide

Description:
5-Amino-N-ethyl-2-methyl-N-phenylbenzenesulfonamide, with the CAS number 51123-09-2, is an organic compound characterized by the presence of an amino group, an ethyl group, and a phenyl group attached to a sulfonamide structure. This compound typically exhibits properties associated with sulfonamides, such as solubility in polar solvents and potential biological activity. The amino group contributes to its basicity, while the sulfonamide moiety can participate in hydrogen bonding, influencing its reactivity and interactions with biological targets. The presence of the ethyl and methyl groups can affect the compound's lipophilicity and steric hindrance, which may play a role in its pharmacological properties. Generally, sulfonamides are known for their antibacterial activity, and derivatives like this one may also exhibit similar properties, making them of interest in medicinal chemistry. However, specific applications and biological activities would require further investigation and validation through experimental studies.
Formula:C15H18N2O2S
InChI:InChI=1S/C15H18N2O2S/c1-3-17(14-7-5-4-6-8-14)20(18,19)15-11-13(16)10-9-12(15)2/h4-11H,3,16H2,1-2H3
InChI key:InChIKey=ZAXMFSSGOARPBM-UHFFFAOYSA-N
SMILES:S(N(CC)C1=CC=CC=C1)(=O)(=O)C2=C(C)C=CC(N)=C2
Synonyms:
  • 4-Toluidine-2-hydroxyethylsulfamide
  • 5-Amino-2-Methyl-N-Ethyl Benzene Sulfonanilide
  • 5-Amino-2-Methyl-N-Ethyl-N-Ethyl Benzene Sulfonanilide
  • 5-Amino-2-Methyl-N-Ethyl-N-Phenylbenzene Sulfonamide
  • 5-Amino-N-Ethyl-2-Methyl-N-Phenylbenzenesulphonamide
  • 5-Amino-N-ethyl-2-toluenesulfonanilide
  • 5-amino-N-ethyl-2-methyl-N-phenylbenzenesulfonamide
  • Benzenesulfonamide, 5-amino-N-ethyl-2-methyl-N-phenyl-
  • NSC 84161
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