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IdentificationBack Directory
[Synonyms]

Propargyl-PEG4-NHBoc
Boc-N-Amido-PEG4-Alkyne
t-Boc-N-Amido-PEG4-propargyl
tert-butyl (3,6,9,12-tetraoxapentadec-14-yn-1-yl)carbamate
tert-butylN-(3,6,9,12-tetraoxapentadec-14-yn-1-yl)carbamate
[MOL File]

1219810-90-8.mol
Chemical PropertiesBack Directory
[Boiling point ]

426.0±40.0 °C(Predicted)
[density ]

1.054±0.06 g/cm3(Predicted)
[solubility ]

Soluble in DMSO, DCM, DMF
[form ]

Liquid
[pka]

12.23±0.46(Predicted)
[color ]

Colorless to light yellow
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Hazard InformationBack Directory
[Description]

t-Boc-N-Amido-PEG4-propargyl is a propargyl linker with one side protected by Boc group. The propargyl group can form triazole linkage with azide-bearing compounds or biomolecules via copper catalyzed Click Chemistry. The Boc protected amine can be deprotected under mild acidic conditions.
[Uses]

Boc-N-Amido-PEG4-propargyl is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Boc-N-Amido-PEG4-propargyl is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide 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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