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Structure of 609-21-2
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2,6-Dibromo-4-aminophenol features two bromine substituents flanking a primary amine and phenolic hydroxyl group, enabling selective functionalization in heterocyclic synthesis. The electron-withdrawing bromines enhance regioselectivity in electrophilic substitution, while the amine and OH groups provide orthogonal reactivity for coupling reactions. This bifunctional scaffold supports efficient access to complex aromatic architectures under mild conditions.
2,6-Dibromo-4-aminophenol serves as a versatile building block for the synthesis of brominated heterocycles and functionalized aromatic scaffolds. Its ortho-bromine substituents enable subsequent cross-coupling reactions, while the phenolic OH and primary amine groups offer orthogonal handles for derivatization. The compound exhibits good bench stability and facilitates efficient purification, making it well-suited for iterative synthesis in medicinal chemistry and materials science applications.
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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: