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Structure of 13073-28-4
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3-Bromo-2-hydroxybenzonitrile features a bromine atom at the meta position relative to the hydroxyl group, creating a unique electronic profile ideal for cross-coupling reactions. The ortho-hydroxy and nitrile functionalities enable chelation and coordination in transition metal catalysis. This bench-stable derivative integrates readily into complex molecular architectures under standard conditions.
3-Bromo-2-hydroxybenzonitrile serves as a versatile building block for the synthesis of functionalized heterocycles and bioactive intermediates. The bromo group enables palladium-catalyzed coupling reactions, while the ortho-hydroxyl and nitrile functionalities offer sites for derivatization, including cyclizations and metal coordination. Its bench-stable nature and compatibility with common protecting group strategies facilitate efficient synthetic planning in medicinal chemistry and process development workflows.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: