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Structure of 67853-37-6
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2-Bromo-3-nitroanisole features a strategically positioned bromine atom and nitro group flanking a methoxy-substituted aromatic ring, enabling direct functionalization in cross-coupling reactions. This electron-deficient aryl halide integrates readily into complex molecular architectures under standard conditions.
2-Bromo-3-nitroanisole serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its well-defined halogen functionality. The nitro group provides strong electron-withdrawing character, enhancing reactivity in nucleophilic substitution and facilitating downstream functionalization. Its methoxy substituent offers orthogonal handle for selective transformations, while the molecule exhibits excellent bench stability and ease of purification—making it a reliable intermediate in the synthesis of complex heterocycles and pharmaceutical scaffolds.
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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: