Maximum quantity allowed is 999
Please select the quantity
CAS RN: 19999-87-2 | Product Number: B3534
Bis(tricyclohexylphosphine)nickel(II) Dichloride
Purity: >95.0%(T)
Synonyms:
- Dichlorobis(tricyclohexylphosphine)nickel(II)
Documents:
Size | Unit Price | Belgium | Japan* | Quantity |
---|---|---|---|---|
1G |
€ 31,00
|
4 | ≥40 |
|
5G |
€ 124,00
|
1 | 24 |
|
*Stock available in Belgium will be delivered in 1 to 3 days
*Stock available in Japan will be delivered in 1 to 2 weeks (excludes regulated items and dry ice shipments).
Specifications
Appearance | Yellow to Amber to Dark red powder to crystal |
Purity(Chelometric Titration) | min. 95.0 % |
Properties (reference)
Melting Point | 227 °C |
GHS
Pictogram |
![]() ![]() |
Signal Word | Danger |
Hazard Statements | H302 : Harmful if swallowed. H372 : Causes damage to organs through prolonged or repeated exposure. H317 : May cause an allergic skin reaction. H334 : May cause allergy or asthma symptoms or breathing difficulties if inhaled. H350 : May cause cancer. |
Precautionary Statements | P260 : Do not breathe dust/ fume/ gas/ mist/ vapours/ spray. P201 : Obtain special instructions before use. P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection. P308 + P313 : IF exposed or concerned: Get medical advice/ attention. P304 + P340 : IF INHALED: Remove person to fresh air and keep comfortable for breathing. |
Related Laws:
Transport Information:
HS Number | 2931599090 |
Application
Nickel Complexes for the Cross-Coupling Reactions Using Alkoxy Groups as Leaving Groups
References
- Activation of Grignard reagents by transition-metal complexes. A new and simple synthesis of trans-stilbenes and polyphenyls
- Selective carbon-carbon bond formation by cross-coupling of Grignard reagents with organic halides. Catalysis by nickel-phosphine complexes
- Nickel-Catalyzed Cross-Coupling of Aryl Grignard Reagents with Aromatic Alkyl Ethers: An Efficient Synthesis of Unsymmetrical Biaryls
Application
Nickel-Catalyzed Cross-Coupling of Aryltrimethylammonium Iodides with Organozinc Reagents
Typical procedure (Ar = Ph, R = 4-CH3Ph): Trimethylphenylammonium iodide (132 mg), bis(tricyclohexylphosphine)nickel(II) dichloride (6.9 mg) and NMP (1.5 mL) are added to a Schlenk tube. To the stirring mixture, 4-CH3C6H4ZnCl solution (1.5 mL, 1.5M solution in THF) is added by a syringe. The reaction mixture is stirred at 90 °C for 8 h and then cooled to room temperature. Water (10 mL) and several drops of acetic acid are successively added. The resulting mixture is extracted with diethyl ether (3 x 10 mL) and the extract is dried over Na2SO4, filtered and concentrated. The residue is purified by column chromatography on silica gel (eluent: petroleum ether or petroleum ether/ethyl acetate 60:1) to give 4-methylbiphenyl (76.5 mg, 91 %).
References
PubMed Literature
Articles/Brochures
TCIMAIL
[TCIMAIL No.148] A Unique and Efficient Ni Catalyst for Cross-Coupling Reactions[Research Articles] Nickel-Catalyzed Cross-Coupling of Aryltrimethylammonium Iodides with Organozinc Reagents
[Product Highlights] Nickel Complexes for the Cross-Coupling Reactions Using Alkoxy Groups as Leaving Groups
Documents (Note: Some products will not have analytical charts available.)
Safety Data Sheet (SDS)
Please select Language.
The requested SDS is not available.
Please Contact Us for more information.
Specifications
C of A & Other Certificates
Please enter Lot Number
Incorrect Lot Number is entered
Analytical Charts
Please enter Lot Number
Incorrect Lot Number is entered
The requested analytical chart is not available. Sorry for the inconvenience.