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Structure of 1226800-12-9
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4-Bromo-2-(difluoromethyl)-6-methylpyridine features a trifunctional pyridine core with distinct reactivity profiles. The bromine at C4 enables palladium-catalyzed cross-coupling, while the difluoromethyl group imparts enhanced metabolic stability and modulates electronic properties. The methyl substituent at C6 provides steric control and improves solubility in organic media. This compound serves as a key intermediate in medicinal chemistry for targeted heterocycle synthesis.
4-Bromo-2-(difluoromethyl)-6-methylpyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its well-defined halogen functionality. The difluoromethyl group imparts enhanced metabolic stability and modulates electronic properties, while the methyl substituent provides steric and electronic tuning. This compound exhibits excellent bench stability and facilitates efficient synthesis of complex heterocyclic scaffolds via standard coupling protocols.
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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: