N-(Azido-PEG3)-N-bis(PEG1-t-butyl ester)

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N-(Azido-PEG3)-N-bis(PEG1-t-butyl ester) Basic information
Product Name:N-(Azido-PEG3)-N-bis(PEG1-t-butyl ester)
Synonyms:N-(Azido-PEG3)-N-bis(PEG1-t-butyl ester);2-(Azido-PEG3-amido)-1,3-bis(t-butyl ester);MUN 89009
CAS:2086689-00-9
MF:C26H48N4O10
MW:576.69
EINECS:
Product Categories:
Mol File:2086689-00-9.mol
N-(Azido-PEG3)-N-bis(PEG1-t-butyl ester) Structure
N-(Azido-PEG3)-N-bis(PEG1-t-butyl ester) Chemical Properties
solubility Soluble in DMSO, DCM. DMF
Safety Information
MSDS Information
N-(Azido-PEG3)-N-bis(PEG1-t-butyl ester) Usage And Synthesis
DescriptionN-(Azido-PEG3)-N-bis(PEG1-t-butyl ester) is developed as a branched PEG linker with a terminal azide group and two t-butyl esters. The azide group enables PEGylation via Click Chemistry. The t-butyl protected carboxyl groups can be deprotected under mild acidic conditions.
UsesN-(Azido-PEG3)-N-bis(PEG1-t-butyl ester) is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. N-(Azido-PEG3)-N-bis(PEG1-t-butyl ester) 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-PEG3)-N-bis(PEG1-t-butyl ester) Preparation Products And Raw materials
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