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Structure of 51933-78-9
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2-Methylthio-5-bromopyridine features a bromine atom at the 5-position and a methylthio group at the 2-position, creating a highly functionalized pyridine scaffold. This electron-deficient heterocycle serves as a key building block in medicinal chemistry, enabling direct coupling reactions via palladium-catalyzed cross-coupling. The thioether moiety enhances solubility and stability compared to analogous halogenated systems.
2-Methylthio-5-bromopyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its bromine substituent. The methylthio group provides orthogonal reactivity and enhances solubility, facilitating downstream functionalization. Bench-stable and readily purified by column chromatography, it functions effectively in the synthesis of heterocyclic scaffolds and biologically active compounds.
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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#: 1759
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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-P330-P501
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Lot numbers can be found on the outside label of a product: