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Structure of 33204-85-2
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2-Bromo-3,4-dimethylpyridine features a brominated pyridine core with two methyl groups positioned at the 3 and 4 positions, enhancing electron density and directing electrophilic substitution. This sterically accessible scaffold integrates readily into cross-coupling reactions, enabling efficient construction of complex heterocyclic architectures under standard conditions.
2-Bromo-3,4-dimethylpyridine serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-established reactivity profile. The bromine atom facilitates efficient C–C bond formation under standard Suzuki, Stille, or Negishi conditions, while the methyl groups enhance solubility and influence electronic properties. Bench-stable and readily purified by recrystallization, it functions as a key intermediate in the construction of substituted pyridine scaffolds relevant to 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-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: