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Structure of 1214326-89-2
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3-Bromo-5-fluoropyridin-4-amine features a pyridine core bearing bromo and fluoro substituents at meta positions relative to the amine, enabling selective cross-coupling and derivatization. The electron-deficient ring facilitates nucleophilic substitution, while the primary amine offers direct functional handles for conjugation. This scaffold delivers high reactivity under standard conditions, supporting rapid access to complex heterocycles in medicinal chemistry and materials science.
3-Bromo-5-fluoropyridin-4-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its complementary halogen reactivity. The bromo group facilitates Suzuki, Stille, and Negishi couplings, while the fluorine enhances metabolic stability and modulates electronic properties. Its amine functionality supports direct derivatization or protection strategies, making it valuable for constructing heterocyclic scaffolds in API development. Bench-stable and readily purified by recrystallization, it integrates seamlessly into multi-step synthetic sequences.
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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: