2,2'-Bis(diphenylphosphino)biphenyl

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Catalog Number
ACM84783642
Product Name
2,2'-Bis(diphenylphosphino)biphenyl
Structure
Structure
CAS
84783-64-2
Category
Organic Phosphine Compounds
Synonyms
BIPHEP; MFCD03094574; AKOS015911364; DB-009479; 1,1'-[[1,1'-BIPHENYL]-2,2'-DIYL]BIS[1,1-DIPHENYL]-PHOSPHINE; CTK3J1519; SCHEMBL1120987; 2,2'-Bis(diphenylphosphino)biphenyl; 2,2'-bis(diphenylphosphanyl)-1,1'-biphenyl; FT-0657577;
IUPAC Name
[2-(2-diphenylphosphanylphenyl)phenyl]-diphenylphosphane;
Molecular Weight
522.568g/mol
Molecular Formula
C36H28P2;
Canonical SMILES
C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3C4=CC=CC=C4P(C5=CC=CC=C5)C6=CC=CC=C6;
InChI
InChI=1S/C36H28P2/c1-5-17-29(18-6-1)37(30-19-7-2-8-20-30)35-27-15-13-25-33(35)34-26-14-16-28-36(34)38(31-21-9-3-10-22-31)32-23-11-4-12-24-32/h1-28H;
InChI Key
GRTJBNJOHNTQBO-UHFFFAOYSA-N;
Application
Supporting ligand in a chiral diamine-ruthenium system for the enantioselective hydrogenation of ketones.

Useful ligand for palladium-catalyzed amination and Kumada cross-coupling reactions

Useful ligand for palladium-catalyzed synthesis of butatrenes.

Useful ligand for iridium-catalyzed C-C cross-coupling of allenes with primary alcohols via transfer hydrogenation.

Useful ligand for iridium-catalyzed C-C cross-coupling of dienes with primary alcohols via transfer hydrogenation.

Useful ligand for iridium-catalyzed C-C cross-coupling of allylic gem-dicarboxylates with aldehydes via transfer hydrogenation.

Useful ligand for the palladium-catalyzed synthesis of chiral allenylsilanes.

Ruthenium-catalyzed synthesis of indoles.

Ruthenium-catalyzed oxidative cyclization.

Rhodium-catalyzed boron arylation.
Complexity
573
Covalently-Bonded Unit Count
1
Exact Mass
522.167g/mol
Heavy Atom Count
38
Monoisotopic Mass
522.167g/mol
Rotatable Bond Count
7
Topological Polar Surface Area
0A^2
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