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Structure of 156361-02-3
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6-Amino-5-chloro-3-pyridinecarbonitrile features a pyridine core functionalized with electron-withdrawing nitrile and chloro groups flanking a primary amine, enabling direct incorporation into heterocyclic scaffolds. This bench-stable derivative serves as a key intermediate in medicinal chemistry, particularly for kinase inhibitor and antiviral agent development.
6-Amino-5-chloro-3-pyridinecarbonitrile serves as a versatile building block in medicinal chemistry, enabling the construction of pyridine-based heterocycles through standard coupling and functional group transformation protocols. Its ortho-substituted nitrile and amino groups provide complementary reactivity for late-stage derivatization, while the chlorine atom facilitates palladium-catalyzed cross-coupling reactions. The compound exhibits good bench stability and is readily purified by recrystallization or chromatography, supporting its use in scalable synthesis workflows.
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GHS Pictogram :
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GHS No : GHS05,GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H315-H318-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P310-P311-P312-P330-P361-P363-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: