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Structure of 87932-50-1
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2-Chloro-3,4-dihydroxybenzoic acid features a chlorinated benzene ring with adjacent hydroxyl groups and a carboxylic acid at the para position, enabling strong hydrogen bonding and enhanced solubility in polar solvents. This configuration supports its use in bioactive molecule synthesis, particularly as a scaffold for kinase inhibitors and antioxidant analogs. The electron-withdrawing chlorine stabilizes reactive intermediates during coupling reactions.
2-Chloro-3,4-dihydroxybenzoic acid serves as a versatile building block in medicinal chemistry and natural product synthesis, enabling the construction of bioactive heterocycles and polyphenolic scaffolds. Its ortho-dihydroxy functionality offers strong metal-chelating capacity, while the chloro and carboxylic acid groups provide sites for selective derivatization via coupling, esterification, or nucleophilic substitution reactions. The compound exhibits good bench stability and facilitates purification through standard chromatographic techniques.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: