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Atomfair 5-Tert-butyl-2-chloropyridine C9H12ClN

Description 5-Tert-butyl-2-chloropyridine (CAS No. 102236-19-1) is a high-purity chlorinated pyridine derivative with the molecular formula C9H12ClN . This compound features a tert-butyl group at the 5-position and a chlorine substituent at the 2-position of the pyridine ring, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its IUPAC name is 5-tert-butyl-2-chloropyridine , and it is also known by synonyms such as 5-(tert-Butyl)-2-chloropyridine and MFCD28040569 . This product is rigorously tested for quality, ensuring optimal performance in research applications. Suitable for use in cross-coupling reactions, ligand synthesis, and as a building block for agrochemicals and active pharmaceutical ingredients (APIs).

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Description

Description

5-Tert-butyl-2-chloropyridine (CAS No. 102236-19-1) is a high-purity chlorinated pyridine derivative with the molecular formula C9H12ClN. This compound features a tert-butyl group at the 5-position and a chlorine substituent at the 2-position of the pyridine ring, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its IUPAC name is 5-tert-butyl-2-chloropyridine, and it is also known by synonyms such as 5-(tert-Butyl)-2-chloropyridine and MFCD28040569. This product is rigorously tested for quality, ensuring optimal performance in research applications. Suitable for use in cross-coupling reactions, ligand synthesis, and as a building block for agrochemicals and active pharmaceutical ingredients (APIs).

  • CAS No: 102236-19-1
  • Molecular Formula: C9H12ClN
  • Molecular Weight: 169.65
  • Exact Mass: 169.0658271
  • Monoisotopic Mass: 169.0658271
  • IUPAC Name: 5-tert-butyl-2-chloropyridine
  • SMILES: CC(C)(C)C1=CN=C(C=C1)Cl
  • Synonyms: 5-tert-butyl-2-chloropyridine, 102236-19-1, 863-765-7, 5-(tert-Butyl)-2-chloropyridine, MFCD28040569

Application

5-Tert-butyl-2-chloropyridine is widely used as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its reactive chlorine and sterically hindered tert-butyl group make it ideal for Suzuki-Miyaura and other cross-coupling reactions. Researchers also employ it in the development of ligands for catalysis and as a precursor for heterocyclic compounds. Its stability and versatility make it a valuable tool in medicinal chemistry and material science.

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