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Dichlorobis(di-t-butylphenylphosphino)palladium(II), 99%

Catalog Number
ACM34409444-3
Product Name
Dichlorobis(di-t-butylphenylphosphino)palladium(II), 99%
Structure
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CAS
34409-44-4
  • Product Overview
  • Usage
Synonyms
QNNRAWADYXIGHE-UHFFFAOYSA-L; SCHEMBL1304876; dichlorobis(di-tert-butylphenylphosphine)palladium(ii); MFCD09953450; AKOS027251097; Y-200033; AK187535; Dichlorobis(di-tert-butylphenylphosphine) palladium(II);
IUPAC Name
ditert-butyl(phenyl)phosphane;dichloropalladium;
Molecular Weight
621.944g/mol
Molecular Formula
C28H46Cl2P2Pd;
Canonical SMILES
CC(C)(C)P(C1=CC=CC=C1)C(C)(C)C.CC(C)(C)P(C1=CC=CC=C1)C(C)(C)C.Cl[Pd]Cl;
InChI
InChI=1S/2C14H23P.2ClH.Pd/c2*1-13(2,3)15(14(4,5)6)12-10-8-7-9-11-12;;;/h2*7-11H,1-6H3;2*1H;/q;;;;+2/p-2;
InChI Key
QNNRAWADYXIGHE-UHFFFAOYSA-L;
Complexity
177
Covalently-Bonded Unit Count
3
Exact Mass
620.149g/mol
Heavy Atom Count
33
Monoisotopic Mass
620.149g/mol
Rotatable Bond Count
6
Topological Polar Surface Area
0A^2
Application
Dichlorobis(di-t-butylphenylphosphino)palladium(II), 99%, is a highly effective pale yellow-white solid catalyst primarily used in facilitating cross-coupling reactions, including the Suzuki-Miyaura coupling reactions. This compound plays a crucial role in organic synthesis by promoting the formation of carbon-carbon bonds, thus serving as an essential tool for chemists in the development of various complex molecules.
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