N-(Azido-PEG2)-N-Boc-PEG4-t-butyl ester

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N-(Azido-PEG2)-N-Boc-PEG4-t-butyl ester Basic information
Product Name:N-(Azido-PEG2)-N-Boc-PEG4-t-butyl ester
Synonyms:N-(Azido-PEG2)-N-Boc-PEG4-t-butyl ester;N-(Azido-PEG2)-N-Boc-PEG4-Boc;WUN 53832;(N3-PEG2)(Boc)-N-PEG4-COOtBu;Boc-(N3-PEG2-CH2CH2)N-PEG4-CH2CH2COOtBu
CAS:2093153-83-2
MF:C26H50N4O10
MW:578.696
EINECS:
Product Categories:
Mol File:2093153-83-2.mol
N-(Azido-PEG2)-N-Boc-PEG4-t-butyl ester Structure
N-(Azido-PEG2)-N-Boc-PEG4-t-butyl ester Chemical Properties
Safety Information
MSDS Information
N-(Azido-PEG2)-N-Boc-PEG4-t-butyl ester Usage And Synthesis
DescriptionN-(Azido-PEG2)-N-Boc-PEG4-t-butyl ester is a very useful branched PEG reagent with a terminal azide group, Boc protected amine, and a terminal t-butyl ester. The azide groups is very reactive with alkyne such as DBCO, BCN and propargyl reagnet via Click Chemistry. The protected amine can be deprotected under acidic conditions, and the t-butyl protected carboxyl group can be deprotected under mild acidic conditions.
UsesN-(Azido-PEG2)-N-Boc-PEG4-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. N-(Azido-PEG2)-N-Boc-PEG4-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; Alkyl/ether
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-PEG2)-N-Boc-PEG4-t-butyl ester Preparation Products And Raw materials
Tag:N-(Azido-PEG2)-N-Boc-PEG4-t-butyl ester(2093153-83-2) Related Product Information
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