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Structure of 39903-01-0
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2-Amino-5-bromo-3-pyridinol features a brominated pyridinol core with complementary amino and hydroxyl functionalities, enabling direct incorporation into heterocyclic scaffolds. This bench-stable derivative serves as a key building block for bioactive molecules in medicinal chemistry and materials science.
2-Amino-5-bromo-3-pyridinol serves as a versatile building block for heterocyclic synthesis, enabling efficient access to functionalized pyridine scaffolds. Its orthogonal reactivity—combining a nucleophilic amino group with a readily displaced bromide—facilitates palladium-catalyzed cross-coupling and electrophilic substitution reactions. The compound exhibits excellent bench stability and is compatible with standard purification protocols, making it well-suited for medicinal chemistry campaigns and process-scale 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: