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BIS(3,5-DI(TRIFLUOROMETHYL)PHENYL)CHLOROPHOSPHINE

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BIS(3,5-DI(TRIFLUOROMETHYL)PHENYL)CHLOROPHOSPHINE Basic information

Product Name:
BIS(3,5-DI(TRIFLUOROMETHYL)PHENYL)CHLOROPHOSPHINE
Synonyms:
  • BIS(3,5-DI(TRIFLUOROMETHYL)PHENYL)CHLOROPHOSPHINE
  • BIS[BIS(3,5-TRIFLUOROMETHYL)PHENYL]CHLOROPHOSPHINE
  • Chlorobis[3,5-bis(trifluoromethyl)phenyl]phosphine, 98+%
  • Chlorobis[3,5-bis(trifluoromethyl)phenyl]phosphine
  • Chlorobis[3,5-bis(trifluoromethyl)phenyl]phosphine, 98+%, may contain suspended dimethylamine hydrochloride crystals
  • P,P-Bis[3,5-bis(trifluoromethyl)phenyl]phosphinous chloride
  • bis[3,5-bis(trifluoromethyl)phenyl]-chlorophosphane
  • Bis(3,5-di(trifluoroMethyl)phenyl)chlorophosphine,Min.98%
CAS:
142421-57-6
MF:
C16H6ClF12P
MW:
492.63
Product Categories:
  • Catalysis and Inorganic Chemistry
  • Phosphorus Compounds
  • Phosphorus Precursors
  • organophosphine ligand
  • Achiral Phosphine
  • Aryl Phosphine
  • P-Cl
Mol File:
142421-57-6.mol
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BIS(3,5-DI(TRIFLUOROMETHYL)PHENYL)CHLOROPHOSPHINE Chemical Properties

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
InChI
1S/C16H6ClF12P/c17-30(11-3-7(13(18,19)20)1-8(4-11)14(21,22)23)12-5-9(15(24,25)26)2-10(6-12)16(27,28)29/h1-6H
InChIKey
DFZQEHBNAJGDCT-UHFFFAOYSA-N
SMILES
FC(F)(F)c1cc(cc(c1)C(F)(F)F)P(Cl)c2cc(cc(c2)C(F)(F)F)C(F)(F)F
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Safety Information

Hazard Codes 
C
Risk Statements 
14-34
Safety Statements 
26-36/37/39-45
RIDADR 
UN3265
WGK Germany 
3
HazardClass 
8
PackingGroup 
II
Storage Class
4.3 - Hazardous materials which set free flammable gases upon contact with water
Hazard Classifications
Skin Corr. 1B
Water-react 3
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BIS(3,5-DI(TRIFLUOROMETHYL)PHENYL)CHLOROPHOSPHINE Usage And Synthesis

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

BIS(3,5-DI(TRIFLUOROMETHYL)PHENYL)CHLOROPHOSPHINESupplier

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