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trans-Bis(dicyclohexylamine)bis(acetato)palladium(II) DAPCy

Catalog Number
ACM628339968-1
Product Name
trans-Bis(dicyclohexylamine)bis(acetato)palladium(II) DAPCy
Structure
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CAS
628339-96-8
  • Product Overview
  • Usage
Synonyms
trans-Bis(dicyclohexylamine)palladium(II) acetate;628339-96-8;DAPCy;Bis(dicyclohexylamino)palladium acetate;MFCD09996893;SC10585;trans-Bis(dicyclohexylamine)bis(acetato)palladium(II) DAPCy;trans-Bis(dicyclohexylamine)palladium(II) acetate, DAPCy;
IUPAC Name
acetic acid;dicyclohexylazanide;palladium(2+);
Molecular Weight
587.154g/mol
Molecular Formula
C28H52N2O4Pd;
Canonical SMILES
CC(=O)O.CC(=O)O.C1CCC(CC1)[N-]C2CCCCC2.C1CCC(CC1)[N-]C2CCCCC2.[Pd+2];
InChI
InChI=1S/2C12H22N.2C2H4O2.Pd/c2*1-3-7-11(8-4-1)13-12-9-5-2-6-10-12;2*1-2(3)4;/h2*11-12H,1-10H2;2*1H3,(H,3,4);/q2*-1;;;+2;
InChI Key
LAYDWGNLLRXNPH-UHFFFAOYSA-N;
Complexity
433
Covalently-Bonded Unit Count
5
Exact Mass
586.296g/mol
H-Bond Acceptor
6
H-Bond Donor
2
Heavy Atom Count
35
Monoisotopic Mass
586.296g/mol
Rotatable Bond Count
4
Topological Polar Surface Area
76.6A^2
Application
trans-Bis(dicyclohexylamine)bis(acetato)palladium(II) DAPCy serves as a highly effective catalyst, designed to facilitate a range of palladium-catalyzed coupling reactions. Its primary applications include the coupling of aryl iodides with triarylbismuths and the synthesis of 3,6-diphenyl-9-hexyl-9H-carbazole derivatives. It is also instrumental in Suzuki coupling reactions, notably with dihexylfluorene derivatives and in Suzuki-Miyaura coupling of dibromopyrone with boronic acids, all under mild aerobic conditions. This versatility makes DAPCy an invaluable tool in the efficient development of complex organic compounds.
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