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*For research and further manufacturing use only, not for direct human use.
Structure of 72093-14-2
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2-Chloro-3,6-dimethylpyridine is a sterically hindered, electron-deficient heterocycle featuring strategically positioned methyl groups that enhance regioselectivity in cross-coupling reactions. This bench-stable scaffold enables efficient construction of complex pyridyl architectures under standard conditions.
2-Chloro-3,6-dimethylpyridine serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling efficient functionalization at the pyridine ring due to its activated halogen and electron-donating methyl groups. Its bench-stable nature and compatibility with palladium-catalyzed cross-coupling reactions facilitate rapid access to substituted pyridine scaffolds common in 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-H320-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: