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Atomfair 2-Hydroxy-5-(trifluoromethyl)pyridine 2H-5TFMP C6H4F3NO

Description 2-Hydroxy-5-(trifluoromethyl)pyridine (CAS No. 33252-63-0) is a high-purity fluorinated pyridine derivative with the molecular formula C6H4F3NO . This compound, also known by its IUPAC name 5-(trifluoromethyl)-1H-pyridin-2-one , features a hydroxyl group at the 2-position and a trifluoromethyl group at the 5-position of the pyridine ring, offering unique electronic and steric properties. Its molecular weight is 163.10 g/mol, and it is supplied as a white to off-white crystalline powder with ??98% purity (HPLC). Ideal for pharmaceutical intermediates, agrochemical synthesis, and material science applications, this compound is packaged under inert gas to ensure stability and longevity. Store in a cool, dry place…

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Description

Description

2-Hydroxy-5-(trifluoromethyl)pyridine (CAS No. 33252-63-0) is a high-purity fluorinated pyridine derivative with the molecular formula C6H4F3NO. This compound, also known by its IUPAC name 5-(trifluoromethyl)-1H-pyridin-2-one, features a hydroxyl group at the 2-position and a trifluoromethyl group at the 5-position of the pyridine ring, offering unique electronic and steric properties. Its molecular weight is 163.10 g/mol, and it is supplied as a white to off-white crystalline powder with ??98% purity (HPLC). Ideal for pharmaceutical intermediates, agrochemical synthesis, and material science applications, this compound is packaged under inert gas to ensure stability and longevity. Store in a cool, dry place away from light and moisture.

  • CAS No: 33252-63-0
  • Molecular Formula: C6H4F3NO
  • Molecular Weight: 163.10
  • Exact Mass: 163.02449824
  • Monoisotopic Mass: 163.02449824
  • IUPAC Name: 5-(trifluoromethyl)-1H-pyridin-2-one
  • SMILES: C1=CC(=O)NC=C1C(F)(F)F
  • Synonyms: 33252-63-0, 2-Hydroxy-5-(trifluoromethyl)pyridine, 2(1H)-Pyridinone, 5-(trifluoromethyl)-, 2H-5TFMP, 5-(Trifluoromethyl)-2(1H)-pyridinone

Application

2-Hydroxy-5-(trifluoromethyl)pyridine serves as a versatile building block in medicinal chemistry for the synthesis of trifluoromethyl-containing bioactive molecules. It is employed in the development of kinase inhibitors and antiviral agents due to its electron-withdrawing trifluoromethyl group. In agrochemical research, it acts as a key intermediate for herbicides and fungicides. The compound’s unique structure also makes it valuable in material science for designing fluorinated polymers and liquid crystals.

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