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Azido-PEG8-t-butyl ester

Base Information Edit
  • Chemical Name:Azido-PEG8-t-butyl ester
  • CAS No.:1623791-99-0
  • Molecular Formula:C23H45N3O10
  • Molecular Weight:523.624
  • Hs Code.:
  • Mol file:1623791-99-0.mol
Azido-PEG8-t-butyl ester

Synonyms:

Suppliers and Price of Azido-PEG8-t-butyl ester
Supply Marketing:Edit
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
  • N3-PEG8-CH2CH2COOtBu min.95%
  • 1 g
  • $ 504.00
  • BroadPharm
  • Azido-PEG8-t-butylester 98%
  • 1 G
  • $ 700.00
  • BroadPharm
  • Azido-PEG8-t-butylester 98%
  • 100 MG
  • $ 230.00
  • BroadPharm
  • Azido-PEG8-t-butylester 98%
  • 500 MG
  • $ 430.00
  • Apolloscientific
  • Azido-PEG8-t-butyl ester
  • 100mg
  • $ 449.00
  • Activate Scientific
  • N3-PEG8-CH2CH2COOtBu 95+%
  • 1 g
  • $ 832.00
  • Acrotein
  • N3-PEG8-CH2CH2COOtBu 97%
  • 0.25g
  • $ 275.00
Total 7 raw suppliers
Chemical Property of Azido-PEG8-t-butyl ester Edit
Chemical Property:
  • Solubility.:Soluble in Water, DMSO, DCM, DMF 
Purity/Quality:

98%,99%, *data from raw suppliers

N3-PEG8-CH2CH2COOtBu min.95% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Description Azido-PEG8-t-butyl ester is a click chemistry compound conpprising an azide group and a t-butyl ester moiety. 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.
Technology Process of Azido-PEG8-t-butyl ester

There total 5 articles about Azido-PEG8-t-butyl ester 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 azide; In acetone; for 16h; Inert atmosphere; Reflux;
DOI:10.1039/c4nj00654b

Reference yield: 98.54%

Guidance literature:
With sodium azide; sodium iodide; In N,N-dimethyl-formamide; at 90 ℃; for 12h;
Guidance literature:
Multi-step reaction with 2 steps
1: triethylamine / dichloromethane / 24 h / 20 °C / Inert atmosphere
2: sodium azide / acetone / 16 h / Inert atmosphere; Reflux
With sodium azide; triethylamine; In dichloromethane; acetone;
DOI:10.1039/c4nj00654b
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