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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. 17791-37-6) is a highly specialized synthetic carbohydrate derivative with the molecular formula C35H38O6. This compound features a tetrahydropyran (oxane) core structure extensively functionalized with methoxy and benzyloxy (phenylmethoxy) groups, making it a valuable intermediate in organic synthesis and carbohydrate chemistry. The presence of multiple benzyl protecting groups enhances its utility in selective glycosylation reactions and complex oligosaccharide assembly. With a molecular weight of 554.68 g/mol, this compound is typically supplied as a white to off-white crystalline powder with high purity (>95%) as confirmed by HPLC and NMR analysis. It is soluble in common organic solvents such…

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Description

Description

2-Methoxy-3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxane (CAS No. 17791-37-6) is a highly specialized synthetic carbohydrate derivative with the molecular formula C35H38O6. This compound features a tetrahydropyran (oxane) core structure extensively functionalized with methoxy and benzyloxy (phenylmethoxy) groups, making it a valuable intermediate in organic synthesis and carbohydrate chemistry. The presence of multiple benzyl protecting groups enhances its utility in selective glycosylation reactions and complex oligosaccharide assembly. With a molecular weight of 554.68 g/mol, this compound is typically supplied as a white to off-white crystalline powder with high purity (>95%) as confirmed by HPLC and NMR analysis. It is soluble in common organic solvents such as dichloromethane, chloroform, and tetrahydrofuran, but insoluble in water. Proper storage at 2-8??C under inert atmosphere is recommended to maintain stability.

  • CAS No: 17791-37-6
  • 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 benzylated carbohydrate derivative serves as a key intermediate in the synthesis of complex oligosaccharides and glycoconjugates, particularly in medicinal chemistry and glycobiology research. It is widely employed in the preparation of protected glycosyl donors for stereoselective glycosylation reactions. Researchers utilize this compound in the development of carbohydrate-based vaccines and antimicrobial agents. The multiple benzyl protecting groups allow for sequential deprotection strategies in multi-step synthetic pathways.

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