Bis(tricyclohexylphosphine)nickel(II) dichloride
Product Information
Molecular Formula
C36H66Cl2NiP2
Molecular Weight
690.46
Description
Catalyst for:• Dehydrobrominative polycondensation• Arylation reactions• Cross-coupling• Suzuki-miyaura cross-coupling reactions• Kumada coupling of diaryl sulfates with Grignard reagents• Olefin dimerization
Synonyms
Bis(tricyclohexylphosphine)nickel(II) Dichloride; dichloronickel; tricyclohexylphosphane; NiCl2(PCy3)2; Nickel, dichlorobis(tricyclohexylphosphine)-; Bis(tricyclohexylphosphine)nickel(II) dichloride, 97%; BIS(TRICYCLOHEXYLPHOSPHINE)NICKEL(II) CHLORIDE; BIS(TRICYCLOHEXYLPHOSPHINE)NICKEL(II) DICHLORIDE; DICHLOROBIS(TRICYCLOHEXYLPHOSPHINE)NICKEL(II)
IUPAC Name
dichloronickeltricyclohexylphosphane
SMILES
C1CCC(CC1)P(C2CCCCC2)C3CCCCC3.C1CCC(CC1)P(C2CCCCC2)C3CCCCC3.Cl[Ni]Cl
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,1-15H22*1H/q+2/p-2
InChI Key
YOCBOYPGZVFUCQ-UHFFFAOYSA-L
Melting Point
284 °C
Flash Point
Not applicable
Purity
97%
Safety Information
Hazards
H302 - H317 - H351
Precautionary Statement
P201 - P280 - P301 + P312 + P330 - P302 + P352 - P308 + P313
Computed Properties
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
6
Exact Mass
688.337023 g/mol
Monoisotopic Mass
688.337023 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
41
Formal Charge
0
Complexity
204
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
3
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-113461509-A | Preparation method of naphthalene ring C-marked alpha-naphthylacetic acid | 2021-07-13 |
| CN-113024340-A | Method for reducing alkyne into olefin by using water as hydrogen source under catalysis of nickel | 2021-03-18 |
| CN-112939728-A | Preparation method of frainer intermediate 1, 3-dichloro-alpha- (trifluoromethyl) styrene | 2021-02-03 |
| CN-112552284-A | Preparation method of chlorantraniliprole | 2020-12-18 |
| CN-112778127-A | Preparation method of flurbiprofen | 2020-06-25 |
| US-2021300884-A1 | Synthesis of oleofurans | 2020-03-24 |
| US-11274088-B2 | Synthesis of oleofurans | 2020-03-24 |
| JP-2021123542-A | Method for Producing Asymmetric Diarylamines | 2020-02-03 |
| CN-110872206-A | Reduction coupling method for synthesizing 1, 1-difluoroethyl aromatic compound | 2019-12-01 |
| JP-2021080401-A | A composition containing a polymer compound, a method for producing the polymer compound, and a method for producing a light emitting element using the polymer compound. | 2019-11-21 |
