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Structure of 6307-87-5
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3-Bromo-5-nitro-benzoic acid methyl ester features a bromine atom at the meta position relative to the carboxylate, paired with a strongly electron-withdrawing nitro group para to the ester. This combination enhances electrophilicity for cross-coupling reactions and provides robust stability under standard conditions. The methyl ester serves as a handle for downstream derivatization, enabling efficient access to functionalized aromatic scaffolds in synthetic chemistry workflows.
3-Bromo-5-nitro-benzoic acid methyl ester serves as a versatile building block in synthetic organic chemistry, enabling the construction of substituted heterocycles and pharmaceutical intermediates. Its defined electronic profile—combining an electron-withdrawing nitro group and a bromo handle—facilitates palladium-catalyzed cross-coupling reactions and directed functionalization. The methyl ester provides a stable, bench-ready platform for further derivatization under standard conditions.
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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: