Atomfair Tetrahydro-3-furanmethanol C5H10O2

Description Tetrahydro-3-furanmethanol (CAS: 15833-61-1) is a high-purity organic compound with the molecular formula C5H10O2, widely used in pharmaceutical and chemical research. This versatile furan derivative, also known by its IUPAC name oxolan-3-ylmethanol , features a hydroxyl-functionalized tetrahydrofuran ring, making it a valuable intermediate in synthetic chemistry. Our product is rigorously tested to ensure ??98% purity (GC), with stringent quality controls for moisture, residual solvents, and heavy metals. Supplied in amber glass bottles under inert gas to prevent degradation, it is ideal for nucleoside synthesis, chiral auxiliaries, and polymer applications. Available in quantities from 1g to 1kg with optional COA/MSDS documentation.

Description

Description

Tetrahydro-3-furanmethanol (CAS: 15833-61-1) is a high-purity organic compound with the molecular formula C5H10O2, widely used in pharmaceutical and chemical research. This versatile furan derivative, also known by its IUPAC name oxolan-3-ylmethanol, features a hydroxyl-functionalized tetrahydrofuran ring, making it a valuable intermediate in synthetic chemistry. Our product is rigorously tested to ensure ??98% purity (GC), with stringent quality controls for moisture, residual solvents, and heavy metals. Supplied in amber glass bottles under inert gas to prevent degradation, it is ideal for nucleoside synthesis, chiral auxiliaries, and polymer applications. Available in quantities from 1g to 1kg with optional COA/MSDS documentation.

  • CAS No: 15833-61-1
  • Molecular Formula: C5H10O2
  • Molecular Weight: 102.13
  • Exact Mass: 102.068079557
  • Monoisotopic Mass: 102.068079557
  • IUPAC Name: oxolan-3-ylmethanol
  • SMILES: C1COCC1CO
  • Synonyms: Tetrahydro-3-furanmethanol, 629-195-6, 15833-61-1, (tetrahydrofuran-3-yl)methanol, oxolan-3-ylmethanol

Application

Tetrahydro-3-furanmethanol serves as a key building block in asymmetric synthesis, particularly for chiral ligand preparation and nucleoside analogs. Its polar aprotic solvent properties are exploited in polymer chemistry for modifying resin solubility. Researchers also utilize it as a precursor for bioactive molecules in pharmaceutical development, including antiviral and anticancer agents.

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