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Dichlorobis(triphenylphosphine)cobalt(II)

Catalog Number
ACM14126400-1
Product Name
Dichlorobis(triphenylphosphine)cobalt(II)
Structure
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CAS
14126-40-0
  • Product Overview
  • Usage
Synonyms
Dichlorobis(triphenylphosphine)cobalt(II); triphenylphosphane; J-007472; 14126-40-0; AC1O0UDG; OPRPFIIIFJLFCE-UHFFFAOYSA-L; MFCD00010010;
IUPAC Name
dichlorocobalt;triphenylphosphane;
Molecular Weight
654.417g/mol
Molecular Formula
C36H30Cl2CoP2;
Canonical SMILES
C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.Cl[Co]Cl;
InChI
InChI=1S/2C18H15P.2ClH.Co/c2*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;;;/h2*1-15H;2*1H;/q;;;;+2/p-2;
InChI Key
OPRPFIIIFJLFCE-UHFFFAOYSA-L;
Complexity
204
Covalently-Bonded Unit Count
3
Exact Mass
653.053g/mol
Heavy Atom Count
41
Monoisotopic Mass
653.053g/mol
Rotatable Bond Count
6
Topological Polar Surface Area
0A^2
Application
Dichlorobis(triphenylphosphine)cobalt(II) serves as a versatile and efficient catalyst across a range of chemical reactions, significantly enhancing the efficiency and outcomes in synthetic chemistry. It is particularly effective in facilitating three-component coupling reactions, such as the cobalt-catalyzed transformation of the alkynyl C-H bond in aldehyde-alkyne-amine coupling processes. Additionally, this catalyst is invaluable in driving reactions including epoxidation, hydrovinylation of styrene, and various cross-coupling and dimerization reactions. It is also utilized in oxidation reactions and as a catalyst for hydrostannations. Furthermore, Dichlorobis(triphenylphosphine)cobalt(II) is crucial in alkyne-dihalomethaneamine couplings, providing an efficient route for the synthesis of propargylamines.
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