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Structure of 586-35-6
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2-Bromoterephthalic acid features a bromine substituent at the para position relative to one carboxylic acid group, enabling selective functionalization in aromatic coupling reactions. This electron-deficient diacid scaffold integrates readily into polymer backbones and serves as a key intermediate for bioconjugation and metal-organic framework synthesis under standard conditions.
2-Bromoterephthalic acid serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions for the construction of functionalized aromatic systems. Its bromo and carboxylic acid functionalities provide orthogonal reactivity, facilitating sequential transformations in complex molecule synthesis. The compound exhibits good bench stability and is readily purified by recrystallization, making it well-suited for use in medicinal chemistry and materials science applications.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: