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Structure of 99132-28-2
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6-Bromo-2,3-dimethylpyridine features a brominated pyridine core with two methyl groups at positions 2 and 3, enabling selective functionalization in cross-coupling reactions. The electron-deficient aromatic ring pairs with the sterically accessible bromine for efficient Pd-catalyzed transformations. This bench-stable derivative serves as a key building block in pharmaceutical synthesis and advanced heterocyclic chemistry.
6-Bromo-2,3-dimethylpyridine serves as a versatile building block in medicinal chemistry and catalytic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-defined halogen functionality. The methyl groups at C2 and C3 provide steric protection and enhance stability, while the pyridine core offers predictable nitrogen coordination for transition metal complexes. This compound facilitates efficient construction of substituted heterocyclic scaffolds with improved bench stability and straightforward purification.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1760
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H318
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Precautionary Statements : P264-P270-P280-P305+P351+P338-P330-P501
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Lot numbers can be found on the outside label of a product: