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Atomfair 5,5,5-Trifluoropentan-1-ol C5H9F3O

Description 5,5,5-Trifluoropentan-1-ol (CAS No. 352-61-4) is a high-purity fluorinated alcohol with the molecular formula C5H9F3O . This compound is characterized by its trifluoromethyl group at the terminal carbon, enhancing its unique physicochemical properties, including increased lipophilicity and metabolic stability. Ideal for pharmaceutical, agrochemical, and material science research, this reagent serves as a versatile building block for synthesizing fluorinated derivatives. Available in various packaging options to suit laboratory-scale and industrial applications, our product undergoes rigorous QC testing (GC, NMR) to ensure ??98% purity. Store under inert conditions to maintain stability.

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Description

Description

5,5,5-Trifluoropentan-1-ol (CAS No. 352-61-4) is a high-purity fluorinated alcohol with the molecular formula C5H9F3O. This compound is characterized by its trifluoromethyl group at the terminal carbon, enhancing its unique physicochemical properties, including increased lipophilicity and metabolic stability. Ideal for pharmaceutical, agrochemical, and material science research, this reagent serves as a versatile building block for synthesizing fluorinated derivatives. Available in various packaging options to suit laboratory-scale and industrial applications, our product undergoes rigorous QC testing (GC, NMR) to ensure ??98% purity. Store under inert conditions to maintain stability.

  • CAS No: 352-61-4
  • Molecular Formula: C5H9F3O
  • Molecular Weight: 142.12
  • Exact Mass: 142.06054939
  • Monoisotopic Mass: 142.06054939
  • IUPAC Name: 5,5,5-trifluoropentan-1-ol
  • SMILES: C(CCO)CC(F)(F)F
  • Synonyms: 5,5,5-trifluoropentan-1-ol, 352-61-4, DTXSID40377829, DTXCID00328857, 860-087-3

Application

5,5,5-Trifluoropentan-1-ol is widely used as an intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals, where its trifluoromethyl group improves bioavailability. It also serves as a precursor for specialty polymers and surfactants due to its hydrophobic properties. Researchers leverage its unique structure in medicinal chemistry for probing enzyme interactions or designing metabolic-resistant compounds.

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