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642091-68-7

642091-68-7 Structure

642091-68-7 Structure
IdentificationBack Directory
[Name]

Azido-PEG4-NHBoc
[CAS]

642091-68-7
[Synonyms]

Boc-NH-PEG3-N3
N3-PEG3-NH-BOC
Azido-PEG3-NHBoc
Azido-PEG4-NHBoc
Boc-N-Amido-PEG3-N3
BocNH-PEG3-CH2CH2N3
Boc-N-Amido-PEG3-Azide
t-Boc-N-Amido-PEG3-Azide
1-Boc-amine-11-azido-3,6,9-trioxaundecane
tert-butyl (2-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)ethyl)carbamate
tert-Butyl N-(2-{2-[2-(2-azidoethoxy)ethoxy]ethoxy}ethyl)carbamate
5,8,11-Trioxa-2-azatridecanoic acid, 13-azido-, 1,1-dimethylethyl ester
[Molecular Formula]

C13H26N4O5
[MDL Number]

MFCD22056317
[MOL File]

642091-68-7.mol
[Molecular Weight]

318.38
Chemical PropertiesBack Directory
[storage temp. ]

Storage temp. 2-8°C
[form ]

Liquid
[color ]

Colorless to light yellow
Hazard InformationBack Directory
[Description]

t-Boc-N-Amido-PEG3-azide is a PEG reagent containing an azide group and Boc-protected amino group, it is reactive with alkyne, BCN, DBCO via Click Chemistry. The Boc group can be deprotected under mild acidic conditions to form the free amine.
[Uses]

Boc-N-Amido-PEG3-azide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Boc-N-Amido-PEG3-azide 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.
[Definition]

ChEBI: Tert-Butyl (2-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)ethyl)carbamate is a carbamate ester.
[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-NHBoc(642091-68-7)1HNMR
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