| Identification | Back Directory | [Name]
Bis(tricyclohexylphosphine)nickel(II) chloride, 99% | [CAS]
19999-87-2 | [Synonyms]
Bis(tricyclohexylphosphine)dichloronickel
Dichlorobis(tricyclohexylphosphine)nickel
Dichlorobis(tricyclohexylphosphine)nickel(II)
Bis(tricyclohexylphosphine)nickel(II) Dichloride
Bis(tricyclohexylphosphine)nickel(II)chloride,99%
Bis(tricyclohexylphosphine)nickel(II) chloride,98%
Bis(tricyclohexylphosphine)nickel(II) chloride, 99%
Bis(tricyclohexylphosphine)nickel(II) dichloride 97%
Bis(tricyclohexylphosphine)nickel(II) chloride,98% (PCy3)2NiCl2 | [Molecular Formula]
2C18H33P.Cl2Ni | [MDL Number]
MFCD11973802 | [MOL File]
19999-87-2.mol | [Molecular Weight]
690.464 |
| Questions And Answer | Back Directory | [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.
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| Hazard Information | Back Directory | [Uses]
Catalyst for:
- Dehydrobrominative polycondensation
- Arylation reactions
- Cross-coupling
- Suzuki-miyaura cross-coupling reactions
- Kumada coupling of diaryl sulfates with Grignard reagents
- Olefin dimerization
| [reaction suitability]
core: nickel
reagent type: catalyst |
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