Tetraethyl decamethylenediphosphonate, 98%
Tetraethyl decamethylenediphosphonate is an organophosphonate linker featuring two phosphonate termini separated by a decamethylene (ten-carbon) spacer, capped as ethyl esters. The phosphonate groups provide strong, chemically addressable handles that can be converted to more reactive phosphonic acid or activated ester forms, enabling controlled conjugation to PROTAC-related building blocks. In targeted protein degradation designs, such linkers are used to tune the three-dimensional distance and relative orientation between the ligand moieties that recruit an E3 ligase and the target-binding warhead, thereby influencing formation of productive ternary complexes. The extended aliphatic chain can reduce steric clashes and improve flexibility, while the diphosphonate functionality supports robust chemical linkage strategies for assembling degraders. As a high-purity linker, it is valuable for researchers optimizing linker length, rigidity, and attachment chemistry to systematically evaluate structure–activity relationships in PROTAC development.
Structure of 5943-62-4
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* For research and manufacturing use only. Not for human or clinical use.
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Tetraethyl decamethylenediphosphonate (high purity grade), provides a chemically robust phosphorus-containing scaffold suitable for assembling bifunctional degraders. Its features support stable linker incorporation and reliable synthetic handling in targeted protein degradation workflows. The subsequent points describe its structure-related characteristics and practical reactivity considerations for constructing PROTAC architectures.
Structure: The linker is a diphosphonate derivative bearing two phosphonate groups and an extended decamethylene-type carbon spacer, capped with ethoxy substituents. It contains P–C and P–O bonds characteristic of phosphonate chemistry, with an overall polar, hydrogen-bonding-capable framework that can engage in stable conjugation strategies.
Reactivity: Phosphonate linkers are commonly used in PROTAC synthesis through phosphorylation/alkylation logic or via conversion to more reactive phosphorus intermediates, enabling formation of P–C or P–O connections to partner ligands. Suitable conditions typically involve dry, inert atmospheres to limit hydrolysis, with base-mediated steps in appropriate organic solvents. Depending on the coupling strategy, catalysts may include standard phosphonate-activation reagents and coupling bases, while aqueous workups are used cautiously to preserve phosphorus functionality.
* 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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