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tert-butyldiphenylsilyl 2-azido-2,6-dideoxy-β-D-glucopyranoside

Base Information Edit
  • Chemical Name:tert-butyldiphenylsilyl 2-azido-2,6-dideoxy-β-D-glucopyranoside
  • CAS No.:1384556-70-0
  • Molecular Formula:C22H29N3O4Si
  • Molecular Weight:427.575
  • Hs Code.:
  • Mol file:1384556-70-0.mol
tert-butyldiphenylsilyl 2-azido-2,6-dideoxy-β-D-glucopyranoside

Synonyms:tert-butyldiphenylsilyl 2-azido-2,6-dideoxy-β-D-glucopyranoside

Suppliers and Price of tert-butyldiphenylsilyl 2-azido-2,6-dideoxy-β-D-glucopyranoside
Supply Marketing:Edit
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of tert-butyldiphenylsilyl 2-azido-2,6-dideoxy-β-D-glucopyranoside Edit
Chemical Property:
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Technology Process of tert-butyldiphenylsilyl 2-azido-2,6-dideoxy-β-D-glucopyranoside

There total 3 articles about tert-butyldiphenylsilyl 2-azido-2,6-dideoxy-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 sodium cyanoborohydride; In diethylene glycol dimethyl ether; for 7h; Reflux;
DOI:10.1016/j.carres.2012.02.015
Guidance literature:
Multi-step reaction with 7 steps
1: pyridine / 20 °C
2: piperidine / tetrahydrofuran / 2.5 h
3: 1H-imidazole / N,N-dimethyl-formamide / 2 h / 60 °C
4: sodium methylate / methanol; dichloromethane
5: pyridine / 2 h / 0 °C
6: sodium iodide / butanone / 6 h / Reflux
7: sodium cyanoborohydride / diethylene glycol dimethyl ether / 7 h / Reflux
With piperidine; 1H-imidazole; sodium methylate; sodium cyanoborohydride; sodium iodide; In tetrahydrofuran; pyridine; methanol; dichloromethane; diethylene glycol dimethyl ether; N,N-dimethyl-formamide; butanone;
DOI:10.1016/j.carres.2012.02.015
Guidance literature:
Multi-step reaction with 8 steps
1: imidazole-1-sulfonyl azide hydrochloride; copper(II) sulfate; triethylamine / methanol / 1.5 h
2: pyridine / 20 °C
3: piperidine / tetrahydrofuran / 2.5 h
4: 1H-imidazole / N,N-dimethyl-formamide / 2 h / 60 °C
5: sodium methylate / methanol; dichloromethane
6: pyridine / 2 h / 0 °C
7: sodium iodide / butanone / 6 h / Reflux
8: sodium cyanoborohydride / diethylene glycol dimethyl ether / 7 h / Reflux
With piperidine; 1H-imidazole; imidazole-1-sulfonyl azide hydrochloride; sodium methylate; sodium cyanoborohydride; copper(II) sulfate; triethylamine; sodium iodide; In tetrahydrofuran; pyridine; methanol; dichloromethane; diethylene glycol dimethyl ether; N,N-dimethyl-formamide; butanone;
DOI:10.1016/j.carres.2012.02.015
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