BocNH-PEG6-CH2CH2N3
BocNH-PEG6-CH2CH2N3 Basic information
- Product Name:
- BocNH-PEG6-CH2CH2N3
- Synonyms:
-
- Azido-PEG6-NHBoc
- BocNH-PEG6-CH2CH2N3
- Boc-NH-PEG6-azide
- Azido-PEG6-Boc Amine
- BocNH-PEG6-CH2CH2N3/5,8,11,14,17,20-Hexaoxa-2-azadocosanoic acid, 22-azido-, 1,1-dimethylethyl ester
- 1-(Boc-amino)-20-azido-3,6,9,12,15,18-hexaoxaicosane
- tert-butyl (20-azido-3,6,9,12,15,18-hexaoxaicosyl)carbamate
- CAS:
- 1292268-15-5
- MF:
- C19H38N4O8
- MW:
- 450.53
- Mol File:
- 1292268-15-5.mol
BocNH-PEG6-CH2CH2N3 Chemical Properties
- storage temp.
- Store at Room Tem.
- solubility
- Soluble in DMSO, DCM, DMF
BocNH-PEG6-CH2CH2N3 Usage And Synthesis
Description
t-boc-N-amido-PEG6-azide is a azide containing crosslinking reagent with a Boc-protected amino group. The hydrophilic PEG spacer increases solubility in aqueous media. The reagent can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The Boc group can be deprotected under mild acidic conditions to form the free amine.
Uses
Boc-NH-PEG6-azide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Boc-NH-PEG6-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
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