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Structure of 2789-92-6
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2-Amino-3,5-dichlorobenzoic acid features a sterically hindered aromatic core with complementary electron-withdrawing chloro groups and a reactive amino functionality. This combination enables direct coupling in peptide synthesis and facilitates conjugation to polymer backbones or biomolecules under mild conditions. The carboxylic acid group provides solubility in polar media and serves as a handle for amide bond formation.
2-Amino-3,5-dichlorobenzoic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles and pharmaceutical intermediates. Its ortho-amino and carboxylic acid functionalities provide orthogonal reactivity for amide coupling, cyclization, and electrophilic substitution reactions. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic workflows in API development.
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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: