Tri(t-butoxycarbonylethoxymethyl) ethanol
Tri(t-butoxycarbonylethoxymethyl) ethanol is a branched multifunctional linker precursor with one alcohol and three protected acids. Structurally, it contains a central carbon framework bearing one free hydroxymethyl group and three carboxyethyl ether arms protected as tert-butyl esters. The alcohol can be activated, etherified, esterified, or converted into another handle, while acidic cleavage of the three tert-butyl esters exposes three carboxylic acids for amide or ester formation; the protecting groups are esters, not tert-butyl carbonates masking hydroxyls. In PROTAC and related targeted protein degradation research, the scaffold supports branched or multivalent conjugate assembly with controlled activation of the central alcohol and acid arms. 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.
Structure of 1027581-61-8
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* For research and manufacturing use only. Not for human or clinical use.
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Tri(t-butoxycarbonylethoxymethyl) ethanol, is designed to serve as a protected, multifunctional alcohol-building block that can be incorporated into targeted protein degradation constructs. Its features support controlled functional-group unveiling and modular conjugation strategies commonly used in PROTAC synthesis. By enabling reliable linker installation and subsequent deprotection steps, it helps researchers prepare well-defined intermediates for assembling ligand–linker–ligand architectures; the detailed structural and reactivity considerations are provided below.
Structure: The linker comprises an ethanol core bearing multiple ethoxymethyl substituents, each masked as a t-butoxycarbonyl (Boc) protected functionality. It contains stable ether and carbon–carbon frameworks alongside ester/urethane-type carbonyl linkages. Overall, it is a protected, polarizable scaffold with latent nucleophilicity revealed after deprotection.
Reactivity: For PROTAC construction, this material is typically used under conditions compatible with Boc chemistry, where acid-mediated deprotection generates free alcohol or related nucleophiles for subsequent coupling. Common approaches rely on controlled acid exposure in suitable organic solvents, followed by base-assisted neutralization and purification. The resulting reactive intermediates can then participate in standard linker–ligand conjugation reactions, such as nucleophilic substitution or ester/ether formation, depending on the partner functional groups.
* 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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