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| | Bis(tricyclohexylphosphine)nickel(II) chloride, 99% Basic information | | Reaction |
| Product Name: | Bis(tricyclohexylphosphine)nickel(II) chloride, 99% | | Synonyms: | Bis(tricyclohexylphosphine)nickel(II) chloride, 99%;Dichlorobis(tricyclohexylphosphine)nickel(II);Bis(tricyclohexylphosphine)nickel(II)chloride,99%;Bis(tricyclohexylphosphine)nickel(II) chloride,98% (PCy3)2NiCl2;Bis(tricyclohexylphosphine)dichloronickel;Bis(tricyclohexylphosphine)nickel(II) chloride,98%;Bis(tricyclohexylphosphine)nickel(II) dichloride 97%;dichloronickel,tricyclohexylphosphane | | CAS: | 19999-87-2 | | MF: | 2C18H33P.Cl2Ni | | MW: | 690.464 | | EINECS: | | | Product Categories: | Ni;metal-phosphine complexes | | Mol File: | 19999-87-2.mol |  |
| | Bis(tricyclohexylphosphine)nickel(II) chloride, 99% Chemical Properties |
| Melting point | 227-231℃ (DEC.) | | storage temp. | Inert atmosphere,Room Temperature | | form | powder to crystal | | color | Yellow to Amber to Dark red | | CAS DataBase Reference | 19999-87-2 |
| | Bis(tricyclohexylphosphine)nickel(II) chloride, 99% Usage And Synthesis |
| Reaction |
- An approach to five-membered lactams from aliphatic amides and terminal acetylenes by nickel catalysis.
- Synthesis of biaryls through nickel-catalyzed Suzuki-Miyaura coupling of amides by carbon-nitrogen bond cleavage.
- Ni-catalyzed borylation of aryl fluorides via C-F cleavage.
- Nickeland palladium–catalyzed coupling of aryl fluorosulfonates with aryl boronic acids enabled by sulfuryl fluoride.
- Nickel-catalyzed one-pot synthesis of biaryls from phenols and arylboronic acids via C-O activation using TCT reagents.
| | Uses | Catalyst for:
- Dehydrobrominative polycondensation
- Arylation reactions
- Cross-coupling
- Suzuki-miyaura cross-coupling reactions
- Kumada coupling of diaryl sulfates with Grignard reagents
- Olefin dimerization
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| | Bis(tricyclohexylphosphine)nickel(II) chloride, 99% Preparation Products And Raw materials |
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