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Atomfair tert-Butyl Dimethylphosphonoacetate C8H17O5P

Description tert-Butyl Dimethylphosphonoacetate (CAS No. 62327-21-3) is a high-purity organophosphorus compound with the molecular formula C8H17O5P . Also known as tert-butyl 2-dimethoxyphosphorylacetate , this versatile reagent is widely used in organic synthesis, particularly in Horner-Wadsworth-Emmons (HWE) reactions for the preparation of ??,??-unsaturated esters. Its stable tert-butyl ester group and reactive phosphonate moiety make it an excellent building block for constructing complex molecular architectures. This product is rigorously tested for purity and consistency, ensuring optimal performance in sensitive applications. Packaged under inert gas to maintain stability, it is ideal for researchers in pharmaceuticals, agrochemicals, and materials science.

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Description

Description

tert-Butyl Dimethylphosphonoacetate (CAS No. 62327-21-3) is a high-purity organophosphorus compound with the molecular formula C8H17O5P. Also known as tert-butyl 2-dimethoxyphosphorylacetate, this versatile reagent is widely used in organic synthesis, particularly in Horner-Wadsworth-Emmons (HWE) reactions for the preparation of ??,??-unsaturated esters. Its stable tert-butyl ester group and reactive phosphonate moiety make it an excellent building block for constructing complex molecular architectures. This product is rigorously tested for purity and consistency, ensuring optimal performance in sensitive applications. Packaged under inert gas to maintain stability, it is ideal for researchers in pharmaceuticals, agrochemicals, and materials science.

  • CAS No: 62327-21-3
  • Molecular Formula: C8H17O5P
  • Molecular Weight: 224.19
  • Exact Mass: 224.08136064
  • Monoisotopic Mass: 224.08136064
  • IUPAC Name: tert-butyl 2-dimethoxyphosphorylacetate
  • SMILES: CC(C)(C)OC(=O)CP(=O)(OC)OC
  • Synonyms: tert-butyl dimethylphosphonoacetate, 629-650-9, 62327-21-3, tert-Butyl 2-(dimethoxyphosphoryl)acetate, tert-Butyl O,O-dimethylphosphonoacetate

Application

tert-Butyl Dimethylphosphonoacetate is primarily employed in the Horner-Wadsworth-Emmons reaction to generate ??,??-unsaturated esters, key intermediates in fine chemical synthesis. It is also used in the preparation of phosphonate-based ligands for catalysis and as a precursor for modified peptides and bioactive molecules. Its stability and reactivity make it valuable in medicinal chemistry for drug discovery and development.

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