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Structure of 376587-53-0
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5-Bromo-3-methyl-2-pyridinecarbaldehyde features a brominated pyridine core with a methyl group at the 3-position and an aldehyde function at the 2-position. This electron-deficient scaffold enables direct coupling in cross-coupling reactions and serves as a key building block for bioactive heterocycles and ligand synthesis under standard conditions.
5-Bromo-3-methyl-2-pyridinecarbaldehyde serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling efficient access to functionalized pyridine scaffolds. Its bromo and aldehyde groups provide orthogonal handles for Suzuki-Miyaura coupling, nucleophilic addition, and condensation reactions, while the methyl group enhances metabolic stability. The compound exhibits good bench stability and is compatible with standard purification techniques, facilitating its use in multi-step syntheses of bioactive molecules 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
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Precautionary Statements : P261-P280-P304+P340-P405
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Lot numbers can be found on the outside label of a product: