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Structure of 2172373-55-4
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This phosphorylated diester integrates a cyanoethoxy-diisopropylamino phosphino group with a pyrimidinone-bearing tetrahydrofuran core, enabling efficient coupling in nucleoside analog synthesis. The molecule exhibits robust stability under standard bench conditions and facilitates selective phosphoramidate formation through its dual ester functionalities.
This compound serves as a protected phosphoramidite building block for oligonucleotide synthesis, enabling efficient coupling in solid-phase DNA and RNA assembly. The cyanoethoxy-dimethylaminophosphino group facilitates rapid deprotection, while the dimethylpropanoate esters ensure bench stability and ease of purification. Its structure supports high-yielding, regioselective phosphotriester formation under standard conditions, making it ideal for scalable nucleic acid synthesis workflows.
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Lot numbers can be found on the outside label of a product: