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t-butyl 20-azido-3,6,9,12,15,18-hexaoxaicosylcarbamate

Base Information
  • Chemical Name:t-butyl 20-azido-3,6,9,12,15,18-hexaoxaicosylcarbamate
  • CAS No.:1292268-15-5
  • Molecular Formula:C19H38N4O8
  • Molecular Weight:450.533
  • Hs Code.:
t-butyl 20-azido-3,6,9,12,15,18-hexaoxaicosylcarbamate

Synonyms:t-butyl 20-azido-3,6,9,12,15,18-hexaoxaicosylcarbamate

Suppliers and Price of t-butyl 20-azido-3,6,9,12,15,18-hexaoxaicosylcarbamate
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • purepeg
  • BocNH-PEG6-CH2CH2N3 min.97%
  • 250 mg
  • $ 200.00
  • BroadPharm
  • t-boc-N-amido-PEG6-azide 98%
  • 1 G
  • $ 450.00
  • BroadPharm
  • t-boc-N-amido-PEG6-azide 98%
  • 500 MG
  • $ 320.00
  • BroadPharm
  • t-boc-N-amido-PEG6-azide 98%
  • 100 MG
  • $ 180.00
  • Activate Scientific
  • BocNH-PEG6-CH2CH2N3 95+%
  • 1 g
  • $ 588.00
  • Acrotein
  • BocNH-PEG6-CH2CH2N3 97%
  • 1g
  • $ 495.00
Total 5 raw suppliers
Chemical Property of t-butyl 20-azido-3,6,9,12,15,18-hexaoxaicosylcarbamate
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

BocNH-PEG6-CH2CH2N3 min.97% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Description t-boc-N-amido-PEG6-azide is a azide containing crosslinking reagent with a Boc-protected amino group. The hydrophilic PEG spacer increases solubility in aqueous media. The reagent can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The Boc group can be deprotected under mild acidic conditions to form the free amine.
Technology Process of t-butyl 20-azido-3,6,9,12,15,18-hexaoxaicosylcarbamate

There total 10 articles about t-butyl 20-azido-3,6,9,12,15,18-hexaoxaicosylcarbamate 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 imidazole-1-sulfonyl azide hydrochloride; copper(ll) sulfate pentahydrate; potassium carbonate; In methanol;
DOI:10.1021/ja411457r
Guidance literature:
Multi-step reaction with 5 steps
1.1: ethanol / 0 - 20 °C
2.1: dmap; triethylamine / dichloromethane / 20 °C / Inert atmosphere
3.1: sodium hydroxide / water; toluene / 1 h / 100 °C
3.2: 20 - 100 °C
4.1: triethylamine / dichloromethane / 0.08 h / 0 °C
4.2: 24 h / 0 - 20 °C
5.1: sodium azide; sodium iodide / water; acetone / 48 h / 80 °C
With dmap; sodium azide; triethylamine; sodium iodide; sodium hydroxide; In ethanol; dichloromethane; water; acetone; toluene;
DOI:10.1002/ejoc.201001666
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