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Structure of 1121586-37-5
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3-Amino-4-bromo-2,6-dichloropyridine features a densely functionalized pyridine core with complementary reactive handles. The amino group enables nucleophilic coupling, while the bromo and dichloro substituents support transition-metal-catalyzed cross-coupling. This scaffold offers high reactivity under standard conditions and excellent stability for use in medicinal chemistry and agrochemical synthesis.
3-Amino-4-bromo-2,6-dichloropyridine serves as a versatile building block in medicinal chemistry and agrochemical synthesis. Its strategically positioned amino, bromo, and dichloro substituents enable selective cross-coupling reactions, nucleophilic substitution, and heterocycle elaboration under standard conditions. The compound exhibits good bench stability and facilitates efficient functionalization for API intermediate development.
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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: