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Structure of 231287-89-1
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6-Bromo-4-nitropicolinic acid features a bromine atom at the 6-position and a nitro group at the 4-position of the picolinic acid scaffold. This electron-deficient heterocycle integrates readily into cross-coupling reactions, serving as a key building block for bioactive molecules and functional materials. The combination of halogen and nitro functionality enables sequential derivatization under mild conditions.
6-Bromo-4-nitropicolinic acid serves as a versatile building block in synthetic organic chemistry, enabling direct functionalization at the pyridine ring via palladium-catalyzed cross-coupling reactions. The bromo group facilitates Suzuki, Stille, and Negishi couplings, while the nitro and carboxylic acid functionalities provide orthogonal handles for further derivatization. Its bench-stable nature and compatibility with standard reaction conditions make it ideal for constructing complex heterocyclic scaffolds and advanced intermediates in medicinal chemistry and materials science.
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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: