N-(Azido-PEG4)-N-Boc-PEG3-t-butyl ester

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N-(Azido-PEG4)-N-Boc-PEG3-t-butyl ester manufacturers

N-(Azido-PEG4)-N-Boc-PEG3-t-butyl ester Basic information
Product Name:N-(Azido-PEG4)-N-Boc-PEG3-t-butyl ester
Synonyms:N-(Azido-PEG4)-N-Boc-PEG3-t-butyl ester;N-Azido-PEG4-N-Boc-N-PEG3-Boc
CAS:2093152-85-1
MF:C28H54N4O11
MW:622.74856
EINECS:
Product Categories:
Mol File:2093152-85-1.mol
N-(Azido-PEG4)-N-Boc-PEG3-t-butyl ester Structure
N-(Azido-PEG4)-N-Boc-PEG3-t-butyl ester Chemical Properties
storage temp. Storage temp. 2-8°C
form Liquid
color Colorless to light yellow
Safety Information
MSDS Information
N-(Azido-PEG4)-N-Boc-PEG3-t-butyl ester Usage And Synthesis
DescriptionN-(Azido-PEG4)-N-Boc-PEG3-t-butyl ester enables Click Chemistry with alkyne such as DBCO , BCN or Propargyl reagent. Boc and the t-butyl protected carboxyl group can be deprotected under mild acidic conditions.
UsesN-Azido-PEG4-N-Boc-N-PEG3-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. N-Azido-PEG4-N-Boc-N-PEG3-Boc is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
IC 50PEGs
References[1] An S, et al. Small-molecule PROTACs: An emerging and promising approach for the development of targeted therapy drugs. EBioMedicine. 2018 Oct;36:553-562 DOI:10.1016/j.ebiom.2018.09.005
N-(Azido-PEG4)-N-Boc-PEG3-t-butyl ester Preparation Products And Raw materials
Tag:N-(Azido-PEG4)-N-Boc-PEG3-t-butyl ester(2093152-85-1) Related Product Information
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