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Atomfair N-(5-bromo-2-methylpyridin-3-yl)acetamide C8H9BrN2O

Description N-(5-bromo-2-methylpyridin-3-yl)acetamide (CAS No. 1301214-71-0) is a high-purity brominated pyridine derivative with the molecular formula C8H9BrN2O . This compound is a valuable intermediate in organic synthesis and pharmaceutical research, featuring a reactive bromine substituent and an acetamide functional group for versatile derivatization. It is supplied as a crystalline solid with ??95% purity (HPLC) and is rigorously tested for consistency, ensuring optimal performance in coupling reactions, heterocycle synthesis, and medicinal chemistry applications. Ideal for researchers developing kinase inhibitors, agrochemicals, or functional materials. Store in a cool, dry place under inert atmosphere to maintain stability.

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Description

Description

N-(5-bromo-2-methylpyridin-3-yl)acetamide (CAS No. 1301214-71-0) is a high-purity brominated pyridine derivative with the molecular formula C8H9BrN2O. This compound is a valuable intermediate in organic synthesis and pharmaceutical research, featuring a reactive bromine substituent and an acetamide functional group for versatile derivatization. It is supplied as a crystalline solid with ??95% purity (HPLC) and is rigorously tested for consistency, ensuring optimal performance in coupling reactions, heterocycle synthesis, and medicinal chemistry applications. Ideal for researchers developing kinase inhibitors, agrochemicals, or functional materials. Store in a cool, dry place under inert atmosphere to maintain stability.

  • CAS No: 1301214-71-0
  • Molecular Formula: C8H9BrN2O
  • Molecular Weight: 229.07
  • Exact Mass: 227.98983
  • Monoisotopic Mass: 227.98983
  • IUPAC Name: N-(5-bromo-2-methylpyridin-3-yl)acetamide
  • SMILES: CC1=C(C=C(C=N1)Br)NC(=O)C
  • Synonyms: N-(5-Bromo-2-methylpyridin-3-yl)acetamide, 1301214-71-0, 818-211-9, Acetamide, N-(5-bromo-2-methyl-3-pyridinyl)-, SCHEMBL1759235

Application

N-(5-bromo-2-methylpyridin-3-yl)acetamide serves as a key building block in Suzuki-Miyaura cross-coupling reactions for pharmaceutical lead optimization. Its bromopyridine core facilitates palladium-catalyzed aryl-aryl bond formation in drug discovery. The compound is also employed in synthesizing kinase-targeting small molecules and as a precursor for functionalized pyridine ligands in catalysis. Researchers utilize it to develop bromine-labeled probes for bioimaging studies.

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