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Structure of 351227-42-4
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6-Chloro-4-iodopyridin-3-amine features a pyridine core functionalized with chlorine and iodine at the 6- and 4-positions, respectively, enabling efficient cross-coupling transformations. The amino group at C3 provides a reactive handle for derivatization, while the electron-withdrawing halogens enhance electrophilicity for palladium-catalyzed reactions. This scaffold demonstrates robust stability under standard conditions and is well-suited for constructing complex heterocyclic architectures in medicinal chemistry and materials science applications.
6-Chloro-4-iodopyridin-3-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its complementary halogen reactivity. The iodine group facilitates efficient Suzuki, Stille, and Negishi couplings, while the chloro substituent offers orthogonal reactivity for sequential functionalization. Its amine functionality enables direct derivatization or incorporation into heterocyclic scaffolds. The compound exhibits good bench stability and is compatible with standard purification methods, making it well-suited for iterative synthesis 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 : 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: