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2353410-03-2

2353410-03-2 Structure

2353410-03-2 Structure
IdentificationBack Directory
[Name]

TCO-PEG8-acid
[CAS]

2353410-03-2
[Synonyms]

TCO-PEG8-acid
[Molecular Formula]

C28H51NO12
[MDL Number]

MFCD31811547
[MOL File]

2353410-03-2.mol
[Molecular Weight]

593.7
Chemical PropertiesBack Directory
[Boiling point ]

686.5±55.0 °C(Predicted)
[density ]

1.15±0.1 g/cm3(Predicted)
[solubility ]

Soluble in Water, DMSO, DCM, DMF
[pka]

4.28±0.10(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
Hazard InformationBack Directory
[Description]

TCO-PEG8-acid is a very reactive click chemistry reagent. The terminal carboxylic acid (CO2H) can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable bond. TCO moiety is reactive with tetrazine-containing compounds to form a stable bond without the catalysis of Cu or elevated temperatures. The inverse-electron demand Diels-Alder cycloaddition reaction of TCO with tetrazines is the fastest bioorthogonal reaction with exceptional selectivity. The hydrophilic PEG spacer increases solubility in aqueous media.
[Uses]

TCO-PEG8-acid is a PEG-based PROTAC linker can be used in the synthesis of PROTACs[1].
[IC 50]

PEGs
[References]

[1] Wang Y, et al. Degradation of proteins by PROTACs and other strategies. Acta Pharm Sin B. 2020 Feb;10(2):207-238. DOI:10.1016/j.apsb.2019.08.001
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