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tert-butyl 3-(2-(2-azidoethoxy)ethoxy)propanoate

Base Information Edit
  • Chemical Name:tert-butyl 3-(2-(2-azidoethoxy)ethoxy)propanoate
  • CAS No.:1271728-79-0
  • Molecular Formula:C11H21N3O4
  • Molecular Weight:259.305
  • Hs Code.:
  • Mol file:1271728-79-0.mol
tert-butyl 3-(2-(2-azidoethoxy)ethoxy)propanoate

Synonyms:

Suppliers and Price of tert-butyl 3-(2-(2-azidoethoxy)ethoxy)propanoate
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
  • Azido-PEG2-t-butylester 98%
  • 1 G
  • $ 450.00
  • Apolloscientific
  • Azido-PEG2- t-butyl ester
  • 100mg
  • $ 292.00
  • Acrotein
  • N3-PEG2-CH2CH2COOtBu 97%
  • 0.25g
  • $ 183.34
  • Absolute Chiral
  • tert-butyl3-(2-(2-azidoethoxy)ethoxy)propanoate 95%
  • 100 mg
  • $ 148.00
  • Absolute Chiral
  • tert-butyl3-(2-(2-azidoethoxy)ethoxy)propanoate 95%
  • 100 mg
  • $ 148.00
Total 9 raw suppliers
Chemical Property of tert-butyl 3-(2-(2-azidoethoxy)ethoxy)propanoate Edit
Chemical Property:
Purity/Quality:

98%,99%, *data from raw suppliers

Azido-PEG2-t-butylester 98% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Description Azido-PEG2- t-butyl ester is a azide containing PEG compound. The azide (N3) group is reactive with BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The t-butyl protected carboxyl group can be deprotected under acidic conditions.
Technology Process of tert-butyl 3-(2-(2-azidoethoxy)ethoxy)propanoate

There total 6 articles about tert-butyl 3-(2-(2-azidoethoxy)ethoxy)propanoate 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 N,N-dimethyl-formamide; at 80 ℃; for 10h;
DOI:10.1002/cbic.202100243
Guidance literature:
With sodium azide; In N,N-dimethyl acetamide; at 80 ℃; for 4h;
Guidance literature:
With diphenylphosphoranyl azide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In N,N-dimethyl-formamide; toluene; at 50 ℃; for 48h; Inert atmosphere;
DOI:10.1021/ja1083915
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