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benzyl 2-azido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside

Base Information Edit
  • Chemical Name:benzyl 2-azido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside
  • CAS No.:342640-42-0
  • Molecular Formula:C27H29N3O5
  • Molecular Weight:475.544
  • Hs Code.:
  • Mol file:342640-42-0.mol
benzyl 2-azido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside

Synonyms:benzyl 2-azido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside

Suppliers and Price of benzyl 2-azido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Total 10 raw suppliers
Chemical Property of benzyl 2-azido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside Edit
Chemical Property:
Purity/Quality:

HPLC≥98% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
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MSDS Files:
Useful:
Technology Process of benzyl 2-azido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside

There total 6 articles about benzyl 2-azido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside 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:
With triethylsilane; boron trifluoride diethyl etherate; In dichloromethane; at 0 ℃; regioselective reaction;
DOI:10.1039/d1sc03188k
Guidance literature:
Multi-step reaction with 2 steps
1: sodium hydride / N,N-dimethyl-formamide / 0 - 20 °C
2: triethylsilane; boron trifluoride diethyl etherate / dichloromethane / 0 °C
With triethylsilane; boron trifluoride diethyl etherate; sodium hydride; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1039/d1sc03188k
Guidance literature:
Multi-step reaction with 5 steps
1: triflic azide; potassium carbonate; copper(II) sulfate / dichloromethane; water / 0 - 20 °C
2: camphor-10-sulfonic acid / acetonitrile
3: silver carbonate / acetonitrile / 60 °C
4: sodium hydride / N,N-dimethyl-formamide / 0 - 20 °C
5: triethylsilane; boron trifluoride diethyl etherate / dichloromethane / 0 °C
With triethylsilane; triflic azide; camphor-10-sulfonic acid; boron trifluoride diethyl etherate; sodium hydride; potassium carbonate; copper(II) sulfate; silver carbonate; In dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1039/d1sc03188k
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