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Atomfair 3,4,5-Trisbenzyloxy-6-benzyloxymethyltetrahydropyran-2-one C34H34O6

Description 3,4,5-Trisbenzyloxy-6-benzyloxymethyltetrahydropyran-2-one (CAS No. 13096-62-3) is a high-purity, synthetic organic compound with the molecular formula C34H34O6. This benzyl-protected lactone derivative is widely utilized in carbohydrate chemistry and pharmaceutical research as a key intermediate for glycosylation reactions and complex oligosaccharide synthesis. The IUPAC name, 3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-one , reflects its intricate tetrahydropyran-2-one core with multiple benzyloxy protective groups. Our product is rigorously characterized by HPLC, NMR, and mass spectrometry to ensure ??95% purity, making it ideal for sensitive applications. Supplied as a white to off-white crystalline powder, it is packaged under inert gas to prevent degradation and shipped with a comprehensive Certificate of…

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Description

Description

3,4,5-Trisbenzyloxy-6-benzyloxymethyltetrahydropyran-2-one (CAS No. 13096-62-3) is a high-purity, synthetic organic compound with the molecular formula C34H34O6. This benzyl-protected lactone derivative is widely utilized in carbohydrate chemistry and pharmaceutical research as a key intermediate for glycosylation reactions and complex oligosaccharide synthesis. The IUPAC name, 3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-one, reflects its intricate tetrahydropyran-2-one core with multiple benzyloxy protective groups. Our product is rigorously characterized by HPLC, NMR, and mass spectrometry to ensure ??95% purity, making it ideal for sensitive applications. Supplied as a white to off-white crystalline powder, it is packaged under inert gas to prevent degradation and shipped with a comprehensive Certificate of Analysis.

  • CAS No: 13096-62-3
  • Molecular Formula: C34H34O6
  • Molecular Weight: 538.6
  • Exact Mass: 538.23553880
  • Monoisotopic Mass: 538.23553880
  • IUPAC Name: 3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-one
  • SMILES: C1=CC=C(C=C1)COCC2C(C(C(C(=O)O2)OCC3=CC=CC=C3)OCC4=CC=CC=C4)OCC5=CC=CC=C5
  • Synonyms: 5-lactone, MFCD08703228, SCHEMBL1087871, BUBVLQDEIIUIQG-UHFFFAOYSA-N, AKOS032947522

Application

This compound serves as a critical building block in the synthesis of complex carbohydrates and glycoconjugates, particularly in the development of glycosidase inhibitors and antiviral agents. Researchers employ it as a protected intermediate for selective deprotection strategies in oligosaccharide assembly. Its benzyl-protected structure enables controlled glycosidic bond formation in medicinal chemistry projects targeting infectious diseases.

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