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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) Dichloride;Bis(tricyclohexylphosphine)nickel(II)chloride,99%;Bis(tricyclohexylphosphine)nickel(II) chloride,98% (PCy3)2NiCl2;Bis(tricyclohexylphosphine)dichloronickel;Dichlorobis(tricyclohexylphosphine)nickel;Bis(tricyclohexylphosphine)nickel(II) chloride,98% | | 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 | | InChI | InChI=1S/2C18H33P.2ClH.Ni/c2*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;;;/h2*16-18H,1-15H2;2*1H;/q;;;;+2/p-2 | | InChIKey | YOCBOYPGZVFUCQ-UHFFFAOYSA-L | | SMILES | C1(CCCCC1)P(C1CCCCC1)C1CCCCC1.C1(CCCCC1)P(C1CCCCC1)C1CCCCC1.Cl[Ni]Cl | | CAS DataBase Reference | 19999-87-2 |
| Hazard Codes | Xn | | Risk Statements | 22-40-43 | | Safety Statements | 53-36/37-45-60 | | WGK Germany | 3 | | HS Code | 2931.90.9051 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Acute Tox. 4 Oral Carc. 2 Skin Sens. 1 |
| | 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
| | reaction suitability | core: nickel reagent type: catalyst |
| | Bis(tricyclohexylphosphine)nickel(II) chloride, 99% Preparation Products And Raw materials |
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