Application

Reactant for:•Enantioselective synthesis of 10-isocyano-4-cadinene and its stereoisomers with antifouling activity•Preparation of 4-Oxo-2-alkenylphosphonates via silylation followed by regiospecific Friedel-Crafts acylation and isomerization

Diethyl (2-methylallyl)phosphonate can be used as a reagent in the Horner-Wadsworth-Emmons reaction to form conjugated carbon–carbon double bonds. It can also be used as a reactant for: Enantioselective total synthesis of 10-isocyano-4-cadinene as antifouling agent. Regiospecific preparation of 4-oxo-2-alkenylphosphonates (OAP) via silylation followed by Friedel-Crafts acylation and isomerization. OAP can serve as building blocks for the construction of polyethylenic chains. The synthesis of azaphosphone as a potent analgesic/anti-inflammatory agents.

General description

Diethyl (2-methylallyl)phosphonate is an organophosphorous compound. It participates in the synthesis of α-aminophosphonate derivatives and azaphosphones. The analgesic/antiinflammatory properties of these derivatives were evaluated.

Packaging

1 g in glass bottle