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Structure of 881891-83-4
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2-Chloro-5-fluoro-4-methylpyridine features a trifunctional pyridine core with orthogonal reactivity, enabling selective transformations in late-stage functionalization. The chloro and fluoro substituents enhance electrophilic susceptibility, while the methyl group provides steric stabilization. This compound serves as a key building block for bioactive heterocycles in medicinal chemistry and agrochemical synthesis.
2-Chloro-5-fluoro-4-methylpyridine serves as a versatile building block in medicinal chemistry, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. Its ortho-chloro and meta-fluoro substituents provide complementary reactivity for selective derivatization, while the methyl group enhances metabolic stability. The compound exhibits excellent bench stability and compatibility with diverse reaction conditions, facilitating rapid access to substituted pyridine scaffolds relevant to pharmaceutical 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: