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Structure of 1260672-14-7
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6-Chloro-3-fluoropyridin-2-amine features a trifunctional heterocyclic core with strategically positioned halogen substituents. The ortho-chloro and meta-fluoro groups enable selective cross-coupling reactions, while the pyridin-2-amine handle facilitates metal coordination and derivatization. This scaffold delivers enhanced reactivity in transition-metal-catalyzed transformations under standard conditions.
6-Chloro-3-fluoropyridin-2-amine serves as a versatile building block in medicinal chemistry, enabling efficient access to fluorinated heterocyclic scaffolds. Its orthogonal halogen functionality facilitates palladium-catalyzed cross-coupling reactions, while the primary amine supports derivatization via acylation, alkylation, or reductive amination. The compound exhibits excellent bench stability and compatibility with standard synthetic workflows, making it well-suited for the construction of kinase inhibitors and other bioactive molecules.
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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: