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Structure of 1016228-01-5
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1-(6-Bromo-3-fluoropyridin-2-yl)ethan-1-one features a bromo-fluoro-substituted pyridine core paired with an acetyl group, delivering a robust scaffold for late-stage functionalization. This electron-deficient heterocycle integrates seamlessly into cross-coupling reactions and enables efficient access to complex pharmaceutical intermediates under standard conditions.
1-(6-Bromo-3-fluoropyridin-2-yl)ethan-1-one serves as a versatile building block in medicinal chemistry, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The ortho-bromo and meta-fluoro substituents provide complementary reactivity for sequential derivatization, while the acetyl group offers a handle for further transformations such as enolization or nucleophilic substitution. Its bench-stable nature and compatibility with standard synthetic workflows make it ideal for constructing complex heterocyclic scaffolds and API intermediates.
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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: