CAS 850429-67-3
:N-benzyl-3-bromo-4-methylbenzenesulfonamide
Description:
N-benzyl-3-bromo-4-methylbenzenesulfonamide is an organic compound characterized by its sulfonamide functional group, which is known for its antibacterial properties. The presence of a benzyl group and a bromo substituent on the aromatic ring contributes to its chemical reactivity and potential applications in medicinal chemistry. The compound features a methyl group that enhances its lipophilicity, potentially influencing its biological activity and solubility. Its structure suggests that it may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, due to the electron-withdrawing nature of the sulfonamide and bromo groups. Additionally, the compound's sulfonamide moiety can form hydrogen bonds, which may play a role in its interactions with biological targets. Overall, N-benzyl-3-bromo-4-methylbenzenesulfonamide is of interest in the field of drug development and research due to its unique structural features and potential pharmacological properties.
Formula:C14H14BrNO2S
InChI:InChI=1/C14H14BrNO2S/c1-11-7-8-13(9-14(11)15)19(17,18)16-10-12-5-3-2-4-6-12/h2-9,16H,10H2,1H3
SMILES:Cc1ccc(cc1Br)S(=O)(=O)NCc1ccccc1
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Found 2 products.
N-Benzyl 3-bromo-4-methylbenzenesulfonamide
CAS:Formula:C14H14BrNO2SColor and Shape:SolidMolecular weight:340.2355N-Benzyl-N-3-bromo-4-methylbenzenesulphonamide
CAS:N-Benzyl-N-3-bromo-4-methylbenzenesulphonamide
Purity:98%Molecular weight:340.24g/mol

