ChemicalBook--->CAS DataBase List--->1092654-47-1

1092654-47-1

1092654-47-1 Structure

1092654-47-1 Structure
IdentificationBack Directory
[Name]

Azido-PEG3-CH2CO2-NHS
[CAS]

1092654-47-1
[Synonyms]

N3-PEG3-CH2COONHS
Azido-PEG3-CH2CO2-NHS
Azido-PEG3-CH2COOH NHS Ester
2,5-dioxopyrrolidin-1-yl 2-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)acetate
[Molecular Formula]

C12H18N4O7
[MDL Number]

MFCD29067172
[MOL File]

1092654-47-1.mol
[Molecular Weight]

330.3
Chemical PropertiesBack Directory
[storage temp. ]

Storage temp. -20°C
[solubility ]

Soluble in Water, DMSO, DCM, DMF
[form ]

Liquid
[color ]

Colorless to light yellow
Hazard InformationBack Directory
[Description]

Azido-PEG3-CH2CO2-NHS consist of azide and NHS ester moieties The azide(N3) group is reactive with alkynes, BCN and DBCO via Click Chemistry to yield a stable triazole linkage. The NHS ester can label the primary amines (-NH2) of proteins, amine-modified oligonucleotides, and other amine-containing molecules.
[Uses]

Azido-PEG3-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Azido-PEG3-NHS 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 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-PEG3-CH2CO2-NHS(1092654-47-1)1HNMR
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