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Structure of 914358-73-9
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3-Amino-5-bromo-2-methylpyridine features a strategically positioned amino group and bromine atom on a pyridine scaffold, enabling selective functionalization in cross-coupling reactions. The methyl substituent enhances electronic modulation and solubility, supporting efficient integration into pharmaceutical intermediates and advanced materials under standard conditions.
3-Amino-5-bromo-2-methylpyridine serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling direct functionalization at multiple sites. The amino group facilitates nucleophilic substitution and coupling reactions, while the bromo substituent supports palladium-catalyzed cross-coupling transformations. Its methyl group enhances metabolic stability and modulates electronic properties. This compound exhibits excellent bench stability and is readily purified by recrystallization or column chromatography, making it ideal for scalable synthesis of pyridine-based pharmaceutical intermediates.
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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: