Tetrakis(triphenylphosphite)nickel(0)

Product Information

Molecular Formula:
[(C6H5O)3P]4Ni
Molecular Weight:
1303.86
Description
Catalyst for alkene and alkyne hydrocyanation and styrenedimerization
Synonyms
Nickel tetrakis(triphenoxyphosphine),Tetrakis(triphenoxyphosphine)nickel,[(PhO)3P]4Ni
IUPAC Name
nickeltriphenyl phosphite
Canonical SMILES
C1=CC=C(C=C1)OP(OC2=CC=CC=C2)OC3=CC=CC=C3.C1=CC=C(C=C1)OP(OC2=CC=CC=C2)OC3=CC=CC=C3.C1=CC=C(C=C1)OP(OC2=CC=CC=C2)OC3=CC=CC=C3.C1=CC=C(C=C1)OP(OC2=CC=CC=C2)OC3=CC=CC=C3.[Ni]
InChI
InChI=1S/4C18H15O3P.Ni/c4*1-4-10-16(11-5-1)19-22(20-17-12-6-2-7-13-17)21-18-14-8-3-9-15-18/h4*1-15H
InChI Key
PGXCIAAANFTEKX-UHFFFAOYSA-N
Melting Point
145 °C (dec.) (lit.)
Flash Point
Not applicable
Storage
2-8°C

Safety Information

Hazards
H315 - H317 - H319 - H335 - H351
Precautionary Statement
P201 - P280 - P302 + P352 - P305 + P351 + P338 - P308 + P313

Computed Properties

Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
12
Rotatable Bond Count
24
Exact Mass
1298.238867 g/mol
Monoisotopic Mass
1298.238867 g/mol
Topological Polar Surface Area
111Ų
Heavy Atom Count
89
Formal Charge
0
Complexity
247
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
5
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CA-3079019-A1 Process for the preparation of 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile 2017-10-10
CN-111263760-A Process for the preparation of 6- (2-hydroxy-2-methylpropoxy) -4- (6- (6- ((6-methoxypyridin-3-yl) methyl) -3, 6-diazabicyclo [3.1.1] hept-3-yl) pyridin-3-yl) pyrazolo [1, 5-a ] pyridine-3-carbonitrile 2017-10-10
US-2019106438-A1 Process for the preparation of 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile 2017-10-10
US-10745419-B2 Process for the preparation of 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile 2017-10-10
US-2020308194-A1 Process for the preparation of 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile 2017-10-10
US-11098064-B2 Process for the preparation of 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbontrile 2017-10-10
US-2021380609-A1 Process for the preparation of 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile 2017-10-10
JP-2018188610-A Method for producing polyarylene sulfide resin composition 2017-04-28
AU-2017316639-A1 Methods for cross coupling 2016-08-23
CA-3032734-A1 Methods for cross coupling 2016-08-23
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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