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4-O-acetyl-5-azido-2-N,3-O-dibenzyl-2,5,6-trideoxy-2,6-imino-β-L-galactose acetyl methyl acetal

Base Information
  • Chemical Name:4-O-acetyl-5-azido-2-N,3-O-dibenzyl-2,5,6-trideoxy-2,6-imino-β-L-galactose acetyl methyl acetal
  • CAS No.:1401914-21-3
  • Molecular Formula:C25H30N4O6
  • Molecular Weight:482.536
  • Hs Code.:
4-O-acetyl-5-azido-2-N,3-O-dibenzyl-2,5,6-trideoxy-2,6-imino-β-L-galactose acetyl methyl acetal

Synonyms:

Suppliers and Price of 4-O-acetyl-5-azido-2-N,3-O-dibenzyl-2,5,6-trideoxy-2,6-imino-β-L-galactose acetyl methyl acetal
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Chemical Property of 4-O-acetyl-5-azido-2-N,3-O-dibenzyl-2,5,6-trideoxy-2,6-imino-β-L-galactose acetyl methyl acetal
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Technology Process of 4-O-acetyl-5-azido-2-N,3-O-dibenzyl-2,5,6-trideoxy-2,6-imino-β-L-galactose acetyl methyl acetal

There total 3 articles about 4-O-acetyl-5-azido-2-N,3-O-dibenzyl-2,5,6-trideoxy-2,6-imino-β-L-galactose acetyl methyl acetal 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:
Multi-step reaction with 3 steps
1: pyridine / dichloromethane / 1 h / -40 °C / Inert atmosphere
2: tetrahydrofuran / 2 h / -30 - 20 °C / Inert atmosphere
3: boron trifluoride diethyl etherate; acetic anhydride / 2.5 h / -30 - 20 °C / Inert atmosphere
With pyridine; boron trifluoride diethyl etherate; acetic anhydride; In tetrahydrofuran; dichloromethane;
DOI:10.1002/chem.201200110
Guidance literature:
Multi-step reaction with 2 steps
1: tetrahydrofuran / 2 h / -30 - 20 °C / Inert atmosphere
2: boron trifluoride diethyl etherate; acetic anhydride / 2.5 h / -30 - 20 °C / Inert atmosphere
With boron trifluoride diethyl etherate; acetic anhydride; In tetrahydrofuran;
DOI:10.1002/chem.201200110
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