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| CUPROUS HYDRIDE TRIPHENYLPHOSPHINE HEXAMER Basic information |
| Product Name: | CUPROUS HYDRIDE TRIPHENYLPHOSPHINE HEXAMER | | Synonyms: | CUPROUS HYDRIDE TRIPHENYLPHOSPHINE HEXAMER;HYDRIDO(TRIPHENYLPHOSPHINE)COPPER(I) HEXAMER;TRIPHENYLPHOSPHINE-COPPER(I) HYDRIDE HEXAMER;(Triphenylphosphine)copper hydride, hexamer, 90%;STRYKER'S REAGENT;Cuprous hydride triphenylphosphine hexamer, Hydrido(triphenylphosphine)copper(I) hexamer, Strykers reagent, Triphenylphosphine-Copper(I) hydride Hexamer;Cuprous hydride triphenylphosphine hexamer, Strykers reagent;Triphenylphosphinecopper(I) hydride hexamer,97% | | CAS: | 33636-93-0 | | MF: | C108H102Cu6P6 | | MW: | 1967.12 | | EINECS: | | Product Categories: | | Mol File: | 33636-93-0.mol |
| CUPROUS HYDRIDE TRIPHENYLPHOSPHINE HEXAMER Chemical Properties |
| Melting point | 111° (dec) | | density | 1.367 | | storage temp. | Refrigerator (+4°C) | | form | Crystals | | color | Red |
| CUPROUS HYDRIDE TRIPHENYLPHOSPHINE HEXAMER Usage And Synthesis |
| Chemical Properties | Red crystals | | Uses | Stoichiometric reducing agent or catalyst in reduction reactions. | | Uses | Stryker’s Reagent is a catalyst for conjugate reduction of ortho-substituted cinnamic esters forming copper enolates. Also used as a catalyst in hydrosilation reactions. | | Uses | Some useful synthetic applications of (Triphenylphosphine)copperhydride hexamer include stoichiometric and catalytic hydrogenations, chemoselective conjugate reductions, as well as regiospecific and stereoselectiveconjugate hydride reductions. | | General Description | Triphenylgermanium hydride is a hydrogen donor. |
| CUPROUS HYDRIDE TRIPHENYLPHOSPHINE HEXAMER Preparation Products And Raw materials |
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