m-PEG5-Boc is a monofunctional, carboxyl-protected PEG spacer. Structurally, it contains a methoxy-capped PEG5 chain ending in a propionic acid protected as a tert-butyl ester. Acidic cleavage of the tert-butyl ester releases the only covalent coupling handle, a carboxylic acid, which can be activated for amide formation with an amine-bearing ligand or for esterification with an alcohol. In PROTAC and related targeted protein degradation research, the methoxy terminus remains nonreactive and the PEG chain can be used to append a defined hydrophilic tail or spacer to a molecular component. Its defined architecture allows researchers to evaluate how linker polarity, flexibility, attachment sequence, and terminal-group selection influence conjugate preparation and the spatial requirements of productive target–E3 ligase engagement. Clear assignment of the protected and reactive groups also supports reproducible reaction planning and systematic comparison of alternative linker designs in research-focused targeted protein degradation workflows.
Structure of 874208-93-2
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m-PEG5-Boc is a polyethylene glycol based PROTAC linker building block designed to provide aqueous compatibility, conformational flexibility, and tunable spacing between targeting and recruiting modules. Its Boc-protected functionality enables controlled synthetic elaboration, supporting modular assembly of degraders where linker length and polarity influence productive ternary complex formation. The following sections describe the structure and the practical reactivity considerations for constructing PROTACs using this linker.
Structure: This linker combines a PEG chain with a Boc-protected functional group, featuring ether linkages along the polyethylene glycol backbone and a carbamate motif from the Boc group. The resulting material is typically hydrophilic and conformationally flexible, with chemical stability under standard organic synthesis conditions.
Reactivity: Boc-protected intermediates are commonly used in stepwise PROTAC synthesis, where deprotection is performed under acid-mediated conditions to reveal a reactive amine for subsequent coupling. The freed amine can then participate in amide or carbamate-forming reactions with activated carboxylic acid derivatives. Mild bases and appropriate coupling reagents are generally selected to preserve the PEG ether chain and maintain linker integrity.
* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2
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