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Structure of 375368-83-5
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3-Bromo-6-fluoro-2-methylpyridine features a sterically accessible pyridine core with complementary halogen and methyl substituents, enabling selective cross-coupling and functionalization in medicinal chemistry. The electron-deficient ring facilitates palladium-catalyzed reactions under standard conditions.
3-Bromo-6-fluoro-2-methylpyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its complementary halogen reactivity. The fluorine and methyl groups provide orthogonal functional handles for further derivatization, while the pyridine core offers stability and favorable electronic properties. Its bench-stable nature and ease of purification support efficient 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 : H315-H319-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: