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Propargyl-PEG4-CH2CO2tBu

Base Information Edit
  • Chemical Name:Propargyl-PEG4-CH2CO2tBu
  • CAS No.:888010-02-4
  • Molecular Formula:C15H26O6
  • Molecular Weight:302.368
  • Hs Code.:
  • Mol file:888010-02-4.mol
Propargyl-PEG4-CH2CO2tBu

Synonyms:tert-butyl-2-(2-{2-[2-(prop-2-ynyloxy)ethoxy]ethoxy}ethoxy)acetate

Suppliers and Price of Propargyl-PEG4-CH2CO2tBu
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
  • BroadPharm
  • Propargyl-PEG4-CH2CO2tBu 98%
  • 250 MG
  • $ 460.00
  • BroadPharm
  • Propargyl-PEG4-CH2CO2tBu 98%
  • 100 MG
  • $ 280.00
  • Apolloscientific
  • Propargyl-PEG4-CH2CO2tBu
  • 100mg
  • $ 546.00
  • Activate Scientific
  • Propargyl-PEG3-CH2COOtBu 97%
  • 1 g
  • $ 464.00
  • Acrotein
  • Propargyl-PEG3-CH2COOtBu 97%
  • 0.5g
  • $ 220.00
  • Abosyn
  • tert-butyl3,6,9,12-tetraoxapentadec-14-yn-1-oate 95%-98%
  • 1g
  • $ 600.00
Total 13 raw suppliers
Chemical Property of Propargyl-PEG4-CH2CO2tBu Edit
Chemical Property:
Purity/Quality:

98%,99%, *data from raw suppliers

Propargyl-PEG4-CH2CO2tBu 98% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Description Propargyl-PEG4-CH2CO2tBu is a PEG reagent that can reacts with azide compounds or biomolecules under the catalyzation of copper. The t-butyl protected carboxyl group can be deprotected under acidic conditions.
Technology Process of Propargyl-PEG4-CH2CO2tBu

There total 4 articles about Propargyl-PEG4-CH2CO2tBu 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 tetrabutyl-ammonium chloride; sodium hydroxide; In dichloromethane; water; at 0 - 20 ℃; for 5h;
Guidance literature:
O-propargyl triethylene glycol; With sodium hydride; In tetrahydrofuran; at 0 - 25 ℃; for 0.5h; Inert atmosphere;
tert-Butyl chloroacetate; In tetrahydrofuran; at 25 ℃; for 12h; Inert atmosphere;
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