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Structure of 800402-12-4
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2-Chloro-5-iodo-4-pyridinamine delivers a uniquely reactive pyridine scaffold bearing orthogonal halogen handles. The chlorine and iodine substituents enable sequential cross-coupling transformations, while the amine group facilitates direct functionalization. This compound serves as a key intermediate in the synthesis of bioactive heterocycles and advanced pharmaceutical candidates.
2-Chloro-5-iodo-4-pyridinamine serves as a versatile building block for the synthesis of functionalized pyridine scaffolds, enabling palladium-catalyzed cross-coupling reactions. The strategically positioned chloro and iodo groups offer orthogonal reactivity for sequential transformations, while the primary amine facilitates derivatization. Its bench-stable nature and compatibility with standard coupling protocols make it well-suited for medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H318
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Precautionary Statements : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: