t-boc-N-amido-PEG9-azide
t-boc-N-amido-PEG9-azide Basic information
- Product Name:
- t-boc-N-amido-PEG9-azide
- Synonyms:
-
- t-boc-N-amido-PEG9-azide
- tert-butyl N-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethyl]carbamate
- BocNH-PEG9-CH2CH2N3
- Boc-NH-PEG9-azide
- Azido-PEG9-Boc Amine
- 5,8,11,14,17,20,23,26,29-Nonaoxa-2-azahentriacontanoic acid, 31-azido-, 1,1-dimethylethyl ester
- N3-PEG9-NHBoc
- CAS:
- 2112731-50-5
- MF:
- C25H50N4O11
- MW:
- 582.69
- Mol File:
- 2112731-50-5.mol
t-boc-N-amido-PEG9-azide Chemical Properties
- solubility
- Soluble in Water, DMSO, DCM, DMF
t-boc-N-amido-PEG9-azide Usage And Synthesis
Description
t-boc-N-amido-PEG9-azide is a PEG reagent with an azide and Boc-protected amino group. The hydrophilic PEG spacer increases solubility in aqueous media. The azide group is reactive with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The Boc group can be deprotected under mild acidic conditions to free the amine.
Uses
Boc-NH-PEG9-azide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Boc-NH-PEG9-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; Alkyl/ether
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
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