142421-57-6

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142421-57-6 Structure

Identification	Back Directory
[Name] BIS(3,5-DI(TRIFLUOROMETHYL)PHENYL)CHLOROPHOSPHINE
[CAS] 142421-57-6
[Synonyms] BIS(3,5-DI(TRIFLUOROMETHYL)PHENYL)CHLOROPHOSPHINE BIS[BIS(3,5-TRIFLUOROMETHYL)PHENYL]CHLOROPHOSPHINE Chlorobis[3,5-bis(trifluoromethyl)phenyl]phosphine Bis(3,5-bis(trifluoromethyl)phenyl)chlorophosphine Bis(3,5-Bis(Trifluoromethyl)Ohenyl)Chlorophosphane bis[3,5-bis(trifluoromethyl)phenyl]-chlorophosphane Chlorobis[3,5-bis(trifluoromethyl)phenyl]phosphine, 98+% Bis(3,5-di(trifluoroMethyl)phenyl)chlorophosphine,Min.98% P,P-Bis[3,5-bis(trifluoromethyl)phenyl]phosphinous chloride Phosphinous chloride, P,P-bis[3,5-bis(trifluoromethyl)phenyl]- High purity CAS 142421-57-6 BIS(3,5-DI(TRIFLUOROMETHYL)PHENYL)CHLOROPHOSPHINE in stock Chlorobis[3,5-bis(trifluoromethyl)phenyl]phosphine, 98+%, may contain suspended dimethylamine hydrochloride crystals
[Molecular Formula] C16H6ClF12P
[MDL Number] MFCD01630852
[MOL File] 142421-57-6.mol
[Molecular Weight] 492.63

Chemical Properties	Back Directory
[Melting point ] 25-29 °C
[Boiling point ] 333.2±42.0 °C(Predicted)
[form ] liquid
[color ] colorless
[Water Solubility ] Reacts with water.
[Sensitive ] Moisture Sensitive

Hazard Information	Back Directory
[Uses] Chlorobis[3,5-bis(trifluoromethyl)phenyl]phosphine is used as a reactant for the synthesis of chiral phosphine-aminophosphine ligands for rhodium-catalyzed asymmetric hydrogenation, ligands for palladium-catalyzed stereoselective allylation reactions, enantioselective hydrogenations, Josiphos analog as catalyst for asymmetric hydrogenation, ligands used in asymmetric hydrovinylation reactions.
[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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