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Atomfair 2-Methoxy-3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxane C35H38O6

Description 2-Methoxy-3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxane (CAS No. 61330-62-9) is a highly specialized synthetic carbohydrate derivative with the molecular formula C35H38O6. This compound features a tetra-O-benzylated pyranoside structure, making it a valuable intermediate in organic synthesis and carbohydrate chemistry. Its fully protected sugar moiety ensures stability during complex reactions, particularly in glycosylation and oligosaccharide synthesis. The product is supplied as a high-purity solid, rigorously characterized by NMR, HPLC, and mass spectrometry to ensure consistency for research applications. Ideal for pharmaceutical development, glycobiology studies, and asymmetric synthesis, this compound is packaged under inert conditions to maintain integrity.

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Description

Description

2-Methoxy-3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxane (CAS No. 61330-62-9) is a highly specialized synthetic carbohydrate derivative with the molecular formula C35H38O6. This compound features a tetra-O-benzylated pyranoside structure, making it a valuable intermediate in organic synthesis and carbohydrate chemistry. Its fully protected sugar moiety ensures stability during complex reactions, particularly in glycosylation and oligosaccharide synthesis. The product is supplied as a high-purity solid, rigorously characterized by NMR, HPLC, and mass spectrometry to ensure consistency for research applications. Ideal for pharmaceutical development, glycobiology studies, and asymmetric synthesis, this compound is packaged under inert conditions to maintain integrity.

  • CAS No: 61330-62-9
  • Molecular Formula: C35H38O6
  • Molecular Weight: 554.7
  • Exact Mass: 554.26683893
  • Monoisotopic Mass: 554.26683893
  • IUPAC Name: 2-methoxy-3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxane
  • SMILES: COC1C(C(C(C(O1)COCC2=CC=CC=C2)OCC3=CC=CC=C3)OCC4=CC=CC=C4)OCC5=CC=CC=C5
  • Synonyms: 2-methoxy-3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxane, METHYL-2,3,4,6-TETRA-O-BENZYL-D-GLUCOPYRANOSIDE, Methyl 2,3,4,6-Tetra-O-benzyl-D-mannopyranoside, METHYL 2,3,4,6-TETRA-O-BENZYL-alpha-D-MANNOPYRANOSIDE, (2R,3S,4S,5R,6S)-3,4,5-Tris(benzyloxy)-2-((benzyloxy)methyl)-6-methoxytetrahydro-2H-pyran

Application

This compound serves as a key building block in the synthesis of complex oligosaccharides and glycoconjugates. Researchers utilize it in glycosylation reactions to study stereoselective bond formation. It is also employed in the development of carbohydrate-based therapeutics and vaccines. Additionally, its benzyl-protected groups make it suitable for multi-step synthetic routes in medicinal chemistry.

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