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Structure of 35623-11-1
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This sulfonamide-substituted benzoic acid features a methylamino group that enhances solubility and modulates electronic properties. The para-positioned sulfonamide moiety provides strong hydrogen-bonding capacity, enabling precise molecular recognition in bioconjugation and medicinal chemistry applications.
3-[(Methylamino)sulphonyl]benzoic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles and pharmaceutically relevant scaffolds. The molecule combines a sulfonamide group with a carboxylic acid functionality, offering orthogonal reactivity for peptide coupling, derivatization, and metal coordination. Its bench-stable nature and compatibility with standard synthetic protocols facilitate efficient incorporation into target molecules during lead optimization campaigns.
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GHS Pictogram :
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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: