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84783-64-2

84783-64-2 Structure

84783-64-2 Structure
IdentificationBack Directory
[Name]

2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL
[CAS]

84783-64-2
[Synonyms]

BIPHEP
98% BIPHEP
2,2'-Bis(diphenylphosphino)-1
2,2'-Bis(diphenylphosphino)bip
2,2'-BIS(DIPHENYLPHOSPHINO)BIPHENYL
2,2’-Bis(diphenylphospino)-1,1’-biphenyl
2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL
2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL,98%
2,2'-Bis(diphenylphosphino)-1,1'-biphenyl
2,2'-Bis(diphenylphosphino)-1,1'-biphenyl,98%BIPHEP
2,2'-Bis(diphenylphosphino)-1,1'-biphenyl, (BIPHEP)
{2-[2-(diphenylphosphanyl)phenyl]phenyl}diphenylphosphane
1,1'-[[1,1'-Biphenyl]-2,2'-diyl]bis[1,1-diphenylphosphine]
PHOSPHINE, 1,1''-[[1,1''-BIPHENYL]-2,2''-DIYL]BIS[1,1-DIPHENYL-
[Molecular Formula]

C36H28P2
[MDL Number]

MFCD03094574
[MOL File]

84783-64-2.mol
[Molecular Weight]

522.56
Chemical PropertiesBack Directory
[Appearance]

white crystalline powder or crystals
[Melting point ]

210-214 °C
[Boiling point ]

635.5±48.0 °C(Predicted)
[form ]

crystal
[color ]

white
Hazard InformationBack Directory
[Chemical Properties]

white crystalline powder or crystals
[Uses]

2,2''-Bis(diphenylphosphino)-1,1’-biphenyl (CAS# 84783-64-2) is a chelating phosphine and has been used to study the effects of bite angles on the chemical and physical properties of transition metal complexes. 2,2''-Bis(diphenylphosphino)-1,1’-biphenyl appears as a catalytic ligand in Ni- and Pd-Catalyzed cross-electrophile coupling reactions to form highly substituted 1,3-dienes.
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38-36
[Safety Statements ]

37/39-26
[TSCA ]

No
[HS Code ]

29310099
Questions And AnswerBack Directory
[Reaction]

  1. Supporting ligand in a chiral diamine-ruthenium system for the enantioselective hydrogenation of ketones.
  2. Useful ligand for palladium-catalyzed amination and Kumada cross-coupling reactions
  3. Useful ligand for palladium-catalyzed synthesis of butatrenes.
  4. Useful ligand for iridium-catalyzed C-C cross-coupling of allenes with primary alcohols via transfer hydrogenation.
  5. Useful ligand for iridium-catalyzed C-C cross-coupling of dienes with primary alcohols via transfer hydrogenation.
  6. Useful ligand for iridium-catalyzed C-C cross-coupling of allylic gem-dicarboxylates with aldehydes via transfer hydrogenation.
  7. Useful ligand for the palladium-catalyzed synthesis of chiral allenylsilanes.
  8. Ruthenium-catalyzed synthesis of indoles.
  9. Ruthenium-catalyzed oxidative cyclization.
  10. Rhodium-catalyzed boron arylation. 
Reactions of 84783-64-2_1
Reactions of 84783-64-2_2
Reactions of 84783-64-2_3
Spectrum DetailBack Directory
[Spectrum Detail]

2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL(84783-64-2)1HNMR
2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL(84783-64-2)31PNMR
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