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Phosphine, bis[3-(trifluoromethyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65796-64-7

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65796-64-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65796-64-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,7,9 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 65796-64:
(7*6)+(6*5)+(5*7)+(4*9)+(3*6)+(2*6)+(1*4)=177
177 % 10 = 7
So 65796-64-7 is a valid CAS Registry Number.

65796-64-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name bis[3-(trifluoromethyl)phenyl]phosphane

1.2 Other means of identification

Product number -
Other names Bis-<3-trifluormethyl-phenyl>-phosphin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:65796-64-7 SDS

65796-64-7Relevant academic research and scientific papers

Iminophosphanes: Synthesis, Rhodium Complexes, and Ruthenium(II)-Catalyzed Hydration of Nitriles

Rong, Mark K.,Van Duin, Koen,Van Dijk, Tom,De Pater, Jeroen J. M.,Deelman, Berth-Jan,Nieger, Martin,Ehlers,Slootweg, J. Chris,Lammertsma, Koop

supporting information, p. 1079 - 1090 (2017/04/21)

Highly stable iminophosphanes, obtained from alkylating nitriles and reaction of the resulting nitrilium ions with secondary phosphanes, were explored as tunable P-monodentate and 1,3-P,N bidentate ligands in rhodium complexes. X-ray crystal structures ar

162. Transition Metal Complexes with Bidentate Ligands Spanning trans-Position. XII. Steric Effects in the Kinetics and Mechanism of Substitutions at Hydride and Methyl Bisphosphine Platinum(II) Complexes

Elding, Lars I.,Kellenberger, Bruno,Venanzi, Luigi M.

, p. 1676 - 1690 (2007/10/02)

Ligand substitution reactions on square-planar platinum(II) compolexes of the types trans-, trans-, trans- (R=H, Me; X=Cl-, I-,; L=PEt3, bis(3-trifluoromethylpheny

Asymmetric Hydroformylation of Vinyl Acetate with DIOP-Type Ligands

Hobbs, Charles F.,Knowles, W. S.

, p. 4422 - 4427 (2007/10/02)

The rhodium-catalyzed hydroformylation of vinyl acetate and related esters was carried out in the presence of chiral phosphine ligands of the DIOP type to give the corresponding optically active 2-(acyloxy)propanal, a precursor for the amino acid threonine.Ligand structure and the ligand/metal ratio were the primary factors controlling asymmetric induction; temperature, CO pressure, and solvent polarity had minor effects.The highest induction efficiencies, up to 51 percent ee, were obtained with the 5H-dibenzophospholyl derivative of DIOP (DIPHOL, 1e).

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