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| | Benzyl (triphenylphosphoranylidene)acetate Basic information |
| Product Name: | Benzyl (triphenylphosphoranylidene)acetate | | Synonyms: | BENZYL (TRIPHENYLPHOSPHORANYLIDENE)ACETATE;LABOTEST-BB LT00452383;Benzyl (triphenylphosphoranylidene)acetate, 97 %;Benzyl 2-(triphenylphosphoranylidene)acetate;(BenzyloxycarbonylMethylene)triphenylphosphorane;Benzyl(triphenylphosphoranylidene)acetate 97%;Acetic acid,2-(triphenylphosphoranylidene)-, phenylMethyl ester;2-(Triphenylphosphoranylidene)acetic acid phenylmethyl ester | | CAS: | 15097-38-8 | | MF: | C27H23O2P | | MW: | 410.44 | | EINECS: | | | Product Categories: | C-C Bond Formation;Olefination;Wittig Reagents | | Mol File: | 15097-38-8.mol |  |
| | Benzyl (triphenylphosphoranylidene)acetate Chemical Properties |
| Melting point | 120-122 °C(lit.) | | Boiling point | 571.1±43.0 °C(Predicted) | | density | 1.19±0.1 g/cm3(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | form | Powder | | color | White to off-white |
| | Benzyl (triphenylphosphoranylidene)acetate Usage And Synthesis |
| Chemical Properties | white to off-white powder | | Uses | Reactant for:
- Tributylphosphine-mediated vinylogous Wittig reactions
- Synthesis of 1,2-dioxanes for antitrypanosomal activity
- Organocatalytic Michael-type reactions / Wittig reactions of phosphorus ylides and unsaturated ketones
- Stereoselective phosphine-catalyzed cycloaddition to form spirocyclopenteneoxindoles
- Enantioselective synthesis of pantothenic acid
- Preparation of phosphorus ylides from phosphoranes and acetic anhydride
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| | Benzyl (triphenylphosphoranylidene)acetate Preparation Products And Raw materials |
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