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Structure of 5847-59-6
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2-Bromo-4-nitrophenol features a bromine substituent at the ortho position relative to a phenolic hydroxyl group, paired with a strongly electron-withdrawing nitro group at the para position. This combination enhances electrophilic reactivity while maintaining bench-stable handling characteristics. The molecule serves as a key intermediate in the synthesis of functionalized aryl compounds, particularly in pharmaceutical and agrochemical development.
2-Bromo-4-nitrophenol serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized aromatic scaffolds. Its ortho-bromine and para-nitro groups offer complementary reactivity for palladium-catalyzed cross-coupling and selective reduction sequences. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis workflows in medicinal chemistry and materials development.
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GHS Pictogram :
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GHS No : GHS07,GHS09
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Signal Word : Warning
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H410
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Precautionary Statements : P264-P270-P273-P330-P391-P501
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Lot numbers can be found on the outside label of a product: