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2353410-01-0

2353410-01-0 Structure

2353410-01-0 Structure
IdentificationBack Directory
[Name]

Methyltetrazine-PEG5-triethoxysilane
[CAS]

2353410-01-0
[Synonyms]

Methyltetrazine-PEG5-triethoxysilane
1-(4-(6-Methyl-1,2,4,5-tetrazin-3-yl)phenoxy)-N-(3-(triethoxysilyl)propyl)-3,6,9,12-tetraoxapentadecan-15-amide
[Molecular Formula]

C29H49N5O9Si
[MDL Number]

MFCD31811540
[MOL File]

2353410-01-0.mol
[Molecular Weight]

639.82
Chemical PropertiesBack Directory
[solubility ]

Soluble in DMSO, DCM, DMF
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

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

Methyltetrazine-PEG5-triethoxysilane is a click chemistry linker containing a triethoxysilane moiety and a methyltetrazine group. Triethoxysilane is commonly used for surface modifications. This reagent can react with TCO-containing compounds to form a stable covalent 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 chain increases the water solubility of a compound in aqueous media.
[Uses]

Methyltetrazine-PEG5-triethoxysilane is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].
[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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