[1,4-BIS(DIPHENYLPHOSPHINO)BUTANE](1,5-CYCLOOCTADIENE)RHODIUM(I) TETRA-FLUOROBORATE manufacturers
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| | [1,4-BIS(DIPHENYLPHOSPHINO)BUTANE](1,5-CYCLOOCTADIENE)RHODIUM(I) TETRA-FLUOROBORATE Basic information | | Reaction |
| Product Name: | [1,4-BIS(DIPHENYLPHOSPHINO)BUTANE](1,5-CYCLOOCTADIENE)RHODIUM(I) TETRA-FLUOROBORATE | | Synonyms: | (1,4-BIS(DIPHENYLPHOSPHINO)BUTANE)(1,5-C YCLOOCTADIENE)RHODIUM(I) BF4, 98%;[bis(diphenylphosphino)butane](cyclooctadiene)rhodium BF4;[1,4-BIS(DIPHENYLPHOSPHINO)BUTANE](1,5-CYCLOOCTADIENE)RHODIUM(I) TETRA-FLUOROBORATE;1,4-Bis(diphenylphosphino)butane(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate, dichloromethane adduct, min. 98%;1,4-Bis(diphenylpyhosphino)butane(1,5-cycloocatdiene)rhodiuM(I)tetrafluoroborate,dichloroMethaneadduct,Min.98%;1,4-Bis(diphenylphosphino)butane(1,5-cyclooctadiene)rhodiuM(I) tetrafluoroborate, dichloroMethane adduct,98%;[1,4-Bis(diphenylphosphino)butane](1,5-cyclooctadiene)rhodiu;[1,4-Bis(diphenylphosphino)butane](1,5-cyclooctadiene)rhodiuM(I) tetrafluoroborate 98% | | CAS: | 79255-71-3 | | MF: | C36H40BF4P2Rh | | MW: | 724.36 | | EINECS: | | | Product Categories: | Rh;organometallic complex;Catalysis and Inorganic Chemistry;Chemical Synthesis;Rhodium | | Mol File: | 79255-71-3.mol | RHODIUM(I) TETRA-FLUOROBORATE Structure](CAS/GIF/79255-71-3.gif) |
| | [1,4-BIS(DIPHENYLPHOSPHINO)BUTANE](1,5-CYCLOOCTADIENE)RHODIUM(I) TETRA-FLUOROBORATE Chemical Properties |
| Melting point | 205 °C (dec.)(lit.) | | form | Powder | | color | orange | | Sensitive | air sensitive | | CAS DataBase Reference | 79255-71-3 |
| | [1,4-BIS(DIPHENYLPHOSPHINO)BUTANE](1,5-CYCLOOCTADIENE)RHODIUM(I) TETRA-FLUOROBORATE Usage And Synthesis |
| Reaction |
- Catalyst used in the intramolecular, hydroamination of olefins.
- Catalyst used for reductive aminations.
| | Uses | [1,4-Bis(diphenylphosphino)butane](1,5-cyclooctadiene)rhodium(I)tetrafluoroborate can be used as a catalyst for the:- Regioselective hydrogenation of thebaine to synthesize tetrahydrothebaine.
- Enantioselective reductive amination of α-ketoacids with benzylamines to synthesize α-N-benzylamino acids.
- Stereoselective hydrogenation of α-(hydroxymethyl)-acrylate derivatives to synthesize 3-hydroxy-2-methylpropanoates.
| | reaction suitability | core: rhodium reagent type: catalyst |
| | [1,4-BIS(DIPHENYLPHOSPHINO)BUTANE](1,5-CYCLOOCTADIENE)RHODIUM(I) TETRA-FLUOROBORATE Preparation Products And Raw materials |
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