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1,3-Bis(dicyclohexylphosphino)propane bis(tetrafluoroborate)

Catalog Number
ACM1002345507-3
Product Name
1,3-Bis(dicyclohexylphosphino)propane bis(tetrafluoroborate)
Structure
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CAS
1002345-50-7
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Synonyms
SY059050; 1,3-Bis(dicyclohexylphosphino)propane bis(tetrafluoroborate), 97%; 1002345-50-7; Propane-1,3-diylbis(dicyclohexylphosphonium) tetrafluoroborate; 1,3-Bis(dicyclohexylphosphonium)propane bis(tetrafluoroborate); 1,3-Bis(dicyclohexylphosphino)propane bis(tetrafluoro borate); CS-W020740; J-000068;
IUPAC Name
dicyclohexyl(3-dicyclohexylphosphaniumylpropyl)phosphanium;ditetrafluoroborate;
Molecular Weight
612.268g/mol
Molecular Formula
C27H52B2F8P2;
Canonical SMILES
[B-](F)(F)(F)F.[B-](F)(F)(F)F.C1CCC(CC1)[PH+](CCC[PH+](C2CCCCC2)C3CCCCC3)C4CCCCC4;
InChI
InChI=1S/C27H50P2.2BF4/c1-5-14-24(15-6-1)28(25-16-7-2-8-17-25)22-13-23-29(26-18-9-3-10-19-26)27-20-11-4-12-21-27;2*2-1(3,4)5/h24-27H,1-23H2;;/q;2*-1/p+2;
InChI Key
XJZAIJGNZUQTAM-UHFFFAOYSA-P;
Complexity
369
Covalently-Bonded Unit Count
3
Exact Mass
612.36g/mol
H-Bond Acceptor
10
Heavy Atom Count
39
Monoisotopic Mass
612.36g/mol
Rotatable Bond Count
8
Topological Polar Surface Area
0A^2
Application
1,3-Bis(dicyclohexylphosphino)propane bis(tetrafluoroborate) serves as a versatile catalyst and ligand in various chemical reactions. It is primarily utilized in the preparation of silacarboxylic acids and acts as an effective ligand for palladium-catalyzed processes. Notably, it facilitates the carbonylation of aryl tosylates and mesylates, as well as the aminocarbonylation of aryl chlorides, both under mild conditions such as atmospheric pressure.
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