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Structure of 5470-65-5
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3-Bromo-4-nitrophenol features a bromine substituent flanked by a nitro group and hydroxyl moiety, creating a uniquely reactive trifunctional scaffold. This electron-deficient phenol integrates readily into cross-coupling reactions and serves as a key intermediate in the synthesis of functionalized aryl compounds. The molecule exhibits enhanced stability under standard bench conditions and displays favorable solubility in common organic solvents.
3-Bromo-4-nitrophenol serves as a versatile building block in medicinal chemistry and materials science, enabling direct functionalization via palladium-catalyzed cross-coupling reactions. Its bromo group facilitates Suzuki, Stille, and Negishi couplings, while the nitro group allows for selective reduction or participation in electrophilic substitution. The compound exhibits bench stability and compatibility with common protecting group strategies, supporting efficient synthesis of complex heterocyclic scaffolds and functionalized aryl derivatives.
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GHS Pictogram :
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GHS No : GHS05,GHS07,GHS09
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Signal Word : Danger
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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-H315-H317-H318-H410
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Precautionary Statements : P261-P264-P270-P272-P273-P280-P302+P352-P330-P362+P364-P391-P501
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Lot numbers can be found on the outside label of a product: