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Structure of 1709-52-0
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4-Amino-N-methylbenzenesulfonamide features a sulfonamide group conjugated to an electron-rich aromatic ring, enabling robust hydrogen bonding and enhanced solubility in polar solvents. The N-methyl substitution improves metabolic stability and reduces basicity compared to the parent amine, facilitating incorporation into bioactive scaffolds. This derivative serves as a key building block in medicinal chemistry for targeted kinase inhibition and antimicrobial agent development.
4-Amino-N-methylbenzenesulfonamide serves as a key building block in sulfonamide-based medicinal chemistry, enabling the synthesis of diverse heterocyclic scaffolds and bioactive compounds. Its amino group facilitates nucleophilic substitution and coupling reactions, while the N-methylsulfonamide moiety offers enhanced metabolic stability and membrane permeability. The compound exhibits good bench stability and is readily purified by recrystallization, supporting its use in multi-step synthetic sequences for pharmaceutical intermediates.
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: