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Structure of 869371-36-8
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N-(3-(Aminomethyl)phenyl)-N-methylmethanesulfonamide features a strategically positioned sulfonamide group that enhances solubility and metabolic stability. The para-aminomethyl aryl moiety enables direct conjugation in bioconjugation workflows, while the N-methyl substitution reduces basicity and improves membrane permeability. This compound serves as a key intermediate in targeted drug discovery campaigns.
N-(3-(Aminomethyl)phenyl)-N-methylmethanesulfonamide serves as a versatile synthetic intermediate for constructing bioactive scaffolds, enabling efficient amide bond formation and functionalization at the ortho-position of an aromatic ring. The methanesulfonamide group provides excellent stability and facilitates purification, while the primary amine functionality supports further derivatization via alkylation, acylation, or coupling reactions. This compound functions reliably in standard peptide and heterocyclic synthesis workflows.
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Lot numbers can be found on the outside label of a product: