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71360-06-0

71360-06-0 Structure

71360-06-0 Structure
IdentificationBack Directory
[Name]

BIS(3,5-DIMETHYLPHENYL)PHOSPHINE
[CAS]

71360-06-0
[Synonyms]

Bis(3,5-dimethyL
98% [(CH3)2C6H3]2PH
Bis(3,5-dimethylphenyl)
bis(3,5-dimethylphenyl)phosphane
Bis(3,5-dimethylphenyi)phosphine
BIS(3,5-DIMETHYLPHENYL)PHOSPHINE
Phosphine, bis(3,5-dimethylphenyl)-
Bis(3,5-dimethylphenyl)phosphine,99%
Bis(3,5-dimethylphenyl)phosphine, 98% (10wt% in hexanes)
Bis(3,5-diMethylphenyl)phosphine, 98% (10% solution in hexanes)
[Molecular Formula]

C16H19P
[MDL Number]

MFCD01074629
[MOL File]

71360-06-0.mol
[Molecular Weight]

242.3
Chemical PropertiesBack Directory
[Boiling point ]

368.8±42.0 °C(Predicted)
[density ]

1.017 g/mL at 25 °C
[refractive index ]

n20/D1.599
[Fp ]

>110℃
[form ]

liquid
[color ]

colorless
[Sensitive ]

air sensitive
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22
[Safety Statements ]

26-36/37/39
[RIDADR ]

UN 3334
[WGK Germany ]

3
[HS Code ]

29319090
Hazard InformationBack Directory
[Chemical Properties]

Colorless liquid
[Uses]

Bis(3,5-dimethylphenyl)phosphine can be used as a reactant to prepare:
  • Iron(II) chiral diimine diphosphine complexes as catalysts for the asymmetric transfer hydrogenation of ketones.
  • The complex of iridium with biphenol phosphite-phosphine bidentate ligand as an asymmetric catalyst for the hydrogenation of N-arylimines.
  • Chiral phosphines with excellent stereoselectivity by 1, 4 addition reaction with α,β-unsaturated aldehydes using a palladium catalyst.
[reaction suitability]

reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: ligand
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