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O-(1-O-acetyl-3,4,5-tri-O-benzyl-β-D-fructopyranosyl)-(2->1)-3,4,5-tri-O-benzyl-β-D-fructopyranosyl fluoride

Base Information
  • Chemical Name:O-(1-O-acetyl-3,4,5-tri-O-benzyl-β-D-fructopyranosyl)-(2->1)-3,4,5-tri-O-benzyl-β-D-fructopyranosyl fluoride
  • CAS No.:880480-69-3
  • Molecular Formula:C56H59FO11
  • Molecular Weight:927.076
  • Hs Code.:
O-(1-O-acetyl-3,4,5-tri-O-benzyl-β-D-fructopyranosyl)-(2->1)-3,4,5-tri-O-benzyl-β-D-fructopyranosyl fluoride

Synonyms:O-(1-O-acetyl-3,4,5-tri-O-benzyl-β-D-fructopyranosyl)-(2->1)-3,4,5-tri-O-benzyl-β-D-fructopyranosyl fluoride

Suppliers and Price of O-(1-O-acetyl-3,4,5-tri-O-benzyl-β-D-fructopyranosyl)-(2->1)-3,4,5-tri-O-benzyl-β-D-fructopyranosyl fluoride
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Chemical Property of O-(1-O-acetyl-3,4,5-tri-O-benzyl-β-D-fructopyranosyl)-(2->1)-3,4,5-tri-O-benzyl-β-D-fructopyranosyl fluoride
Chemical Property:
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MSDS Files:
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Technology Process of O-(1-O-acetyl-3,4,5-tri-O-benzyl-β-D-fructopyranosyl)-(2->1)-3,4,5-tri-O-benzyl-β-D-fructopyranosyl fluoride

There total 5 articles about O-(1-O-acetyl-3,4,5-tri-O-benzyl-β-D-fructopyranosyl)-(2->1)-3,4,5-tri-O-benzyl-β-D-fructopyranosyl fluoride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
methoxymethyl O-(1-O-acetyl-3,4,5-tri-O-benzyl-β-D-fructopyranosyl)-(2->1)-3,4,5-tri-O-benzyl-β-D-fructopyranoside; With trimethylsilyl bromide; 4 A molecular sieve; In dichloromethane; at 20 ℃; for 0.25h;
With diethylamino-sulfur trifluoride; In dichloromethane; at 20 ℃; for 1h;
DOI:10.3987/COM-05-S(K)54
Guidance literature:
Multi-step reaction with 3 steps
1.1: 81.8 percent / diethylaminosulfur trifluoride / CH2Cl2 / 1 h / 20 °C
2.1: 57.2 percent / zirconocene dichloride; 4 Angstroem molecular sieves; AgClO4 / CH2Cl2 / 2.5 h / 20 °C
3.1: trimethylsilyl bromide; 4 Angstroem molecular sieves / CH2Cl2 / 0.25 h / 20 °C
3.2: 33.6 percent / diethylaminosulfur trifluoride / CH2Cl2 / 1 h / 20 °C
With trimethylsilyl bromide; diethylamino-sulfur trifluoride; 4 A molecular sieve; zirconocene dichloride; silver perchlorate; In dichloromethane;
DOI:10.3987/COM-05-S(K)54
Guidance literature:
Multi-step reaction with 2 steps
1.1: 57.2 percent / zirconocene dichloride; 4 Angstroem molecular sieves; AgClO4 / CH2Cl2 / 2.5 h / 20 °C
2.1: trimethylsilyl bromide; 4 Angstroem molecular sieves / CH2Cl2 / 0.25 h / 20 °C
2.2: 33.6 percent / diethylaminosulfur trifluoride / CH2Cl2 / 1 h / 20 °C
With trimethylsilyl bromide; 4 A molecular sieve; zirconocene dichloride; silver perchlorate; In dichloromethane;
DOI:10.3987/COM-05-S(K)54
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