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Structure of 5093-70-9
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4-Bromo-2,6-dimethylpyridine features a sterically hindered pyridine core with electron-deficient character, enabling selective coupling reactions. The bromine at the 4-position serves as a reliable handle for palladium-catalyzed transformations, while methyl groups at C2 and C6 enhance stability and solubility in organic media.
4-Bromo-2,6-dimethylpyridine serves as a versatile building block in medicinal chemistry and catalysis, enabling palladium-catalyzed cross-coupling reactions due to its stable bromine substituent and electron-deficient pyridine core. The 2,6-dimethyl groups provide steric protection and enhance bench stability, facilitating straightforward purification and scalability. It functions effectively in Suzuki-Miyaura, Stille, and Negishi couplings for constructing complex 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: