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Structure of 1093879-46-9
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This brominated pyridine-acetic acid derivative features a reactive carboxylic acid group flanked by a brominated heteroaryl moiety, enabling direct coupling in cross-coupling or functionalization workflows. The electron-deficient pyridine ring enhances regioselectivity in palladium-catalyzed transformations, while the bench-stable structure simplifies handling and integration into synthetic sequences.
2-(6-Bromopyridin-2-yl)acetic acid serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its brominated pyridine moiety. The carboxylic acid group facilitates direct derivatization or salt formation, enhancing solubility and purification. Its bench-stable nature and compatibility with standard synthetic protocols make it ideal for constructing 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: