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Structure of 38876-67-4
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2-Bromo-6-nitrobenzoic acid features a bromine atom and a nitro group positioned ortho to the carboxylic acid, creating a highly electron-deficient aromatic core. This configuration enables direct functionalization in cross-coupling reactions and facilitates derivatization for bioconjugation or materials synthesis under standard conditions.
2-Bromo-6-nitrobenzoic acid serves as a versatile building block in synthetic organic chemistry, enabling direct functionalization at the aromatic ring through 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 crystalline form allows for straightforward handling and purification, making it well-suited for multi-step synthesis of heterocyclic scaffolds and bioactive molecules.
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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: