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Structure of 3510-66-5
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2-Bromo-5-methylpyridine has been used as starting reagent for the synthesis of:5,5-dimethyl-2,2-bipyridine5-methyl-2,2:6,2-terpyridine5-bromo-5-methyl-2,2:6,2-terpyridine
2-Bromo-5-methylpyridine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions such as Suzuki, Stille, and Negishi couplings. The bromine atom provides high reactivity under standard conditions, while the methyl group enhances regioselectivity in electrophilic substitution and contributes to favorable solubility and bench stability. This compound functions reliably in the construction of complex pyridyl scaffolds relevant to medicinal chemistry and agrochemical 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: