ChemicalBook--->CAS DataBase List--->2112737-90-1

2112737-90-1

2112737-90-1 Structure

2112737-90-1 Structure
IdentificationBack Directory
[Name]

t-Boc-N-Amido-PEG7-propargyl
[CAS]

2112737-90-1
[Synonyms]

Propargyl-PEG7-NHBoc
Boc-NH-PEG7-propargyl
t-Boc-N-Amido-PEG7-propargyl
tert-Butyl 3,6,9,12,15,18,21-heptaoxatetracos-23-yn-1-ylcarbamate
[Molecular Formula]

C22H41NO9
[MDL Number]

MFCD30828698
[MOL File]

2112737-90-1.mol
[Molecular Weight]

463.56
Chemical PropertiesBack Directory
[Boiling point ]

532.7±50.0 °C(Predicted)
[density ]

1.072±0.06 g/cm3(Predicted)
[form ]

Liquid
[pka]

12.23±0.46(Predicted)
[color ]

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

Exclamation Mark (GHS07)
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-PEG7-propargyl is a crosslinking reagent that enables the formation of triazole linkage with azides under the catalyzation of copper. The Boc-protected amine can be deprotected under mild acidic conditions. By introducing PEG chain into the molecule, the hydrophilicity can be greatly improved.
[Uses]

Boc-NH-PEG7-propargyl is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Boc-NH-PEG7-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
[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]

t-Boc-N-Amido-PEG7-propargyl(2112737-90-1)1HNMR
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