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1-azido-2-(2-(2-(2-iodoethyoxy)ethoxy)ethoxy)ethane

Base Information
  • Chemical Name:1-azido-2-(2-(2-(2-iodoethyoxy)ethoxy)ethoxy)ethane
  • CAS No.:936917-36-1
  • Molecular Formula:C8H16IN3O3
  • Molecular Weight:329.138
  • Hs Code.:
1-azido-2-(2-(2-(2-iodoethyoxy)ethoxy)ethoxy)ethane

Synonyms:1-azido-2-(2-(2-(2-iodoethyoxy)ethoxy)ethoxy)ethane

Suppliers and Price of 1-azido-2-(2-(2-(2-iodoethyoxy)ethoxy)ethoxy)ethane
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
  • Matrix Scientific
  • Iodo-PEG3-azide 95%
  • 2.500g
  • $ 1816.00
  • BroadPharm
  • Iodo-PEG3-Azide 98%
  • 1 G
  • $ 780.00
  • BroadPharm
  • Iodo-PEG3-Azide 98%
  • 500 MG
  • $ 540.00
  • BroadPharm
  • Iodo-PEG3-Azide 98%
  • 250 MG
  • $ 350.00
  • A1 Biochem Labs
  • Iodo-PEG3-Azide 95%
  • 2.5 g
  • $ 1100.00
Total 6 raw suppliers
Chemical Property of 1-azido-2-(2-(2-(2-iodoethyoxy)ethoxy)ethoxy)ethane
Chemical Property:
Purity/Quality:

98%,99%, *data from raw suppliers

Iodo-PEG3-azide 95% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Description Iodo-PEG3-Azide is a PEG linker containing iodide and azide moieties. The hydrophilic PEG spacer increases solubility in aqueous media. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The iodide is a very good leaving group for nucleophilic substitution reactions.
Technology Process of 1-azido-2-(2-(2-(2-iodoethyoxy)ethoxy)ethoxy)ethane

There total 5 articles about 1-azido-2-(2-(2-(2-iodoethyoxy)ethoxy)ethoxy)ethane 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 iodide; In acetone; at 65 ℃; for 15h;
DOI:10.1039/c2ob26968f
Guidance literature:
With sodium azide; tetrabutylammomium bromide; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1016/j.ejmech.2019.111859
Guidance literature:
Multi-step reaction with 4 steps
1: silver(l) oxide / dichloromethane / 24 h / 0 - 20 °C
2: sodium azide / N,N-dimethyl-formamide / 12 h / 65 °C
3: triethylamine / dichloromethane / 3.5 h / 0 - 20 °C
4: sodium iodide / acetone / 15 h / 65 °C
With sodium azide; triethylamine; sodium iodide; silver(l) oxide; In dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.1039/c2ob26968f
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