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1421933-29-0

1421933-29-0 Structure

1421933-29-0 Structure
IdentificationBack Directory
[Name]

Azido-PEG4-Amido-tri-(t-butoxycarbonylethoxymethyl)-methane
[CAS]

1421933-29-0
[Synonyms]

Azido-PEG4-Amido-tri-(t-butoxycarbonylethoxymethyl)-methane
[Molecular Formula]

C36H66N4O14
[MDL Number]

MFCD22574791
[MOL File]

1421933-29-0.mol
[Molecular Weight]

778.94
Chemical PropertiesBack Directory
[form ]

Liquid
[color ]

Colorless to light yellow
Hazard InformationBack Directory
[Description]

Azido-PEG4-Amido-tri-(t-butoxycarbonylethoxymethyl)-methane is a branched PEGylation compound with a terminal azide group and three t-butyl groups. The t-butyl groups can be removed under acidic conditions. The azide group can participate in copper-catalyzed Click Chemistry reactions with alkynes, DBCO and BCN to form stable triazole linkages. The hydrophilic PEG linker increases the water solubility of compounds in aqueous media.
[Uses]

Azido-PEG4-Amido-tri-(t-butoxycarbonylethoxymethyl)-methane is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Azido-PEG4-Amido-tri-(t-butoxycarbonylethoxymethyl)-methane 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 50]

PEGs
[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
Spectrum DetailBack Directory
[Spectrum Detail]

Azido-PEG4-Amido-tri-(t-butoxycarbonylethoxymethyl)-methane(1421933-29-0)1HNMR
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