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Structure of 221297-82-1
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3-Bromo-4-chloropyridin-2-amine serves as a critical heterocyclic building block in medicinal chemistry, featuring a pyridine core functionalized with bromo and chloro substituents at adjacent positions. This combination enables selective cross-coupling reactions, particularly palladium-catalyzed variants, facilitating the rapid assembly of complex molecular architectures. The amine group provides a handle for further derivatization, enhancing its utility in drug discovery workflows.
3-Bromo-4-chloropyridin-2-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The bromo group facilitates Suzuki-Miyaura and Buchwald-Hartwig couplings, while the chloro substituent offers enhanced stability under reaction conditions. Its pyridinamine functionality provides a handle for further functionalization and improves solubility in polar solvents. This compound exhibits good bench stability and is compatible with standard purification protocols, making it a reliable intermediate for constructing heterocyclic scaffolds 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: