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Structure of 3512-75-2
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4-Chloro-2,6-dimethylpyridine is a sterically hindered, electron-deficient pyridine derivative featuring orthogonal functional groups that enable selective transformations. This bench-stable heterocycle integrates readily into cross-coupling and metal-ligand frameworks, offering predictable reactivity in synthetic sequences.
4-Chloro-2,6-dimethylpyridine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, offering enhanced reactivity due to the combined electronic effects of the chloro and methyl substituents. Its bench-stable nature and compatibility with palladium-catalyzed cross-coupling reactions enable efficient construction of complex heterocyclic scaffolds. The ortho-methyl groups provide steric protection and improve solubility, facilitating purification and downstream functionalization.
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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: