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Structure of 34552-15-3
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2-Chloro-3-fluoro-5-methylpyridine is a halogenated pyridine derivative featuring complementary chlorine and fluorine substituents at adjacent positions, enabling selective functionalization in medicinal chemistry. The methyl group at the 5-position enhances lipophilicity and metabolic stability. This scaffold integrates readily into bioactive molecules through cross-coupling reactions and serves as a key building block for pharmaceutical intermediates requiring precise electronic tuning and steric control under standard conditions.
2-Chloro-3-fluoro-5-methylpyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The strategically positioned chloro and fluoro groups facilitate sequential functionalization, while the methyl substituent enhances lipophilicity and metabolic stability. This compound exhibits bench stability and compatibility with standard reaction conditions, making it well-suited for the synthesis of heterocyclic scaffolds and API 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: