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Structure of 58584-92-2
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2-Amino-6-chloronicotinic acid features a chlorinated pyridine core with complementary amino and carboxylic acid functionalities, enabling direct integration into bioactive molecule scaffolds. This bench-stable derivative supports efficient coupling reactions and serves as a key building block in medicinal chemistry campaigns targeting heterocyclic pharmacophores.
2-Amino-6-chloronicotinic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles and pharmaceutical intermediates. Its ortho-amino and chloro substituents facilitate directed metalation, Suzuki-Miyaura coupling, and nucleophilic substitution reactions. The compound exhibits good bench stability and is compatible with standard purification methods, 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: