ChemicalBook--->CAS DataBase List--->1144106-65-9

1144106-65-9

1144106-65-9 Structure

1144106-65-9 Structure
IdentificationBack Directory
[Name]

Bromo-PEG1-azide
[CAS]

1144106-65-9
[Synonyms]

Bromo-PEG1-azide
Bromo-PEG1-C2-azide
Bromo-PEG1-azide, Bromo-PEG1-N3
1-azido-2-(2-bromoethoxy)ethane
1-Azido-2-(2-bromoethoxy)ethane/Bromo-PEG1-C2-azide
[Molecular Formula]

C4H8BrN3O
[MDL Number]

MFCD24454187
[MOL File]

1144106-65-9.mol
[Molecular Weight]

194.03
Chemical PropertiesBack Directory
[storage temp. ]

Storage temp. 2-8°C
[solubility ]

Soluble in DMSO, DCM, DMF
[form ]

Liquid
[color ]

Colorless to light yellow
Hazard InformationBack Directory
[Description]

Bromo-PEG1-azide is a bifunctional PEG linker with a bromide (Br)group and an azide(N3) group. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The bromide (Br) is a good leaving group for nucleophilic substitution reactions.
[Uses]

Bromo-PEG1-C2-azide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Bromo-PEG1-C2-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.
[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]

Bromo-PEG1-azide(1144106-65-9)1HNMR
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