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Structure of 84249-14-9
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2-Amino-4-bromopyridine features a bromine substituent at the 4-position and an amino group at the 2-position, creating a uniquely activated pyridine scaffold. This electronic configuration enables direct coupling reactions with palladium catalysts under standard conditions. The compound serves as a key building block in medicinal chemistry for synthesizing kinase inhibitors and bioactive heterocycles.
2-Amino-4-bromopyridine serves as a versatile building block in medicinal chemistry and catalytic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal reactivity profile. The amino group facilitates direct functionalization or protection strategies, while the bromine atom provides a reliable handle for C–C bond formation under standard Suzuki, Stille, or Negishi conditions. Its bench-stable crystalline form simplifies handling and purification, making it well-suited for modular heterocycle construction and API intermediate 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-H317-H319-H335-H412
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Precautionary Statements : P271-P280-P261-P302+P352-P305+P351+P338-P333+P313-P405-P403+P233-P501
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Lot numbers can be found on the outside label of a product: