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Structure of 4793-22-0
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4-Chloro-2-fluoro-5-sulfamylbenzoic acid features a strategically positioned sulfamyl group that enhances solubility and hydrogen-bonding capacity, while the ortho-halogen substituents impart electronic modulation and metabolic stability. This combination enables efficient coupling in pharmaceutical synthesis workflows under standard conditions.
4-Chloro-2-fluoro-5-sulfamylbenzoic acid serves as a versatile building block for bioactive heterocycles and pharmaceutical intermediates, offering orthogonal reactivity between the carboxylic acid, sulfamyl, and halogen functional groups. Its stability under standard synthetic conditions enables straightforward derivatization via amide coupling, Suzuki-Miyaura cross-coupling, or nucleophilic aromatic substitution, facilitating efficient access to complex scaffolds in medicinal chemistry 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: