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Atomfair 2-Bromo-4-methoxypyridine C6H6BrNO

Description 2-Bromo-4-methoxypyridine (CAS No. 118289-16-0) is a high-purity heterocyclic organic compound with the molecular formula C6H6BrNO . This versatile building block features a pyridine core substituted with a bromine atom at the 2-position and a methoxy group at the 4-position, offering excellent reactivity for cross-coupling reactions and nucleophilic substitutions. Ideal for pharmaceutical intermediates, agrochemical synthesis, and material science applications, our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied as a white to off-white crystalline powder. Packaged under inert gas to prevent degradation, each batch includes comprehensive analytical documentation (GC/MS, NMR, HPLC). Available in research (1g, 5g,…

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Description

Description

2-Bromo-4-methoxypyridine (CAS No. 118289-16-0) is a high-purity heterocyclic organic compound with the molecular formula C6H6BrNO. This versatile building block features a pyridine core substituted with a bromine atom at the 2-position and a methoxy group at the 4-position, offering excellent reactivity for cross-coupling reactions and nucleophilic substitutions. Ideal for pharmaceutical intermediates, agrochemical synthesis, and material science applications, our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied as a white to off-white crystalline powder. Packaged under inert gas to prevent degradation, each batch includes comprehensive analytical documentation (GC/MS, NMR, HPLC). Available in research (1g, 5g, 10g) and bulk quantities (100g, 1kg) with custom synthesis options upon request.

  • CAS No: 118289-16-0
  • Molecular Formula: C6H6BrNO
  • Molecular Weight: 188.02
  • Exact Mass: 186.96328
  • Monoisotopic Mass: 186.96328
  • IUPAC Name: 2-bromo-4-methoxypyridine
  • SMILES: COC1=CC(=NC=C1)Br
  • Synonyms: 2-Bromo-4-methoxypyridine, 89488-29-9, DTXSID70406217, DTXCID80357069, 800-556-1

Application

2-Bromo-4-methoxypyridine serves as a key intermediate in Suzuki-Miyaura and Stille cross-coupling reactions for constructing biaryl systems in drug discovery. Its electron-rich pyridine core facilitates palladium-catalyzed aminations in the synthesis of kinase inhibitors and antiviral agents. The compound is also employed in the development of liquid crystal materials and as a directing group in C-H functionalization chemistry.

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