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Structure of 866807-26-3
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Methyl 3-amino-6-chloropicolinate features a chlorine-substituted pyridine core with complementary amino and ester functionalities, enabling direct incorporation into heterocyclic scaffolds. The para-chloro group enhances electrophilic reactivity, while the ortho-amino moiety supports metal coordination and derivatization under mild conditions. This bench-stable intermediate facilitates efficient access to bioactive nitrogen heterocycles in medicinal chemistry workflows.
Methyl 3-amino-6-chloropicolinate serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C3 amine and C6 chlorine sites. Its stability under standard conditions facilitates straightforward derivatization via nucleophilic substitution or coupling reactions. The methyl ester group supports further transformation to carboxylic acids or amides, while the ortho-chloro and amino functionalities enable sequential modification in heterocyclic scaffold construction.
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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: