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| (ACETYLMETHYLENE)TRIPHENYLPHOSPHORANE Basic information |
| (ACETYLMETHYLENE)TRIPHENYLPHOSPHORANE Chemical Properties |
| Melting point | 203-205 °C (lit.) | | Boiling point | 478.5±28.0 °C(Predicted) | | density | 1.14 | | storage temp. | Inert atmosphere,Room Temperature | | solubility | Soluble in chloroform. Slightly soluble in methanol. | | form | Powder | | color | White to off-white | | Sensitive | Air Sensitive | | BRN | 750077 | | Stability: | Stable. Combustible. Incompatible with strong oxidizing agents. | | CAS DataBase Reference | 1439-36-7(CAS DataBase Reference) |
| Risk Statements | 22-36/37/38 | | Safety Statements | 22-24/25 | | WGK Germany | 3 | | RTECS | UC3900000 | | HS Code | 29319090 |
| (ACETYLMETHYLENE)TRIPHENYLPHOSPHORANE Usage And Synthesis |
| Chemical Properties | white to light beige crystalline powder | | Uses | Wittig Reagent | | Uses | (Acetylmethylene)triphenylphosphorane is used as a Wittig reagent in synthetic chemistry, especially for the synthesis of functionalized pyrrolidines and cyclobutanones. It plays as a vital role in asymmetric allylboration for enantioselective synthesis of (+)-awajanomycin.It is also employed as a reactant in the preparation of 1,2-dioxanes with antitrypanosomal activity. Further, it is used in the preparation of amphibian pyrrolizidine alkaloids through allylic aminations and silicon-containing acyclic dienone musk odorants. In addition to this, it is involved in Domino Suzuki/Heck coupling reactions to prepare fluorenylidenes. |
| (ACETYLMETHYLENE)TRIPHENYLPHOSPHORANE Preparation Products And Raw materials |
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