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HRh(CO)(P(C6H4-4-CF3)3)3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

226957-34-2

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226957-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 226957-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,9,5 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 226957-34:
(8*2)+(7*2)+(6*6)+(5*9)+(4*5)+(3*7)+(2*3)+(1*4)=162
162 % 10 = 2
So 226957-34-2 is a valid CAS Registry Number.

226957-34-2Relevant academic research and scientific papers

Investigation of the hydroformylation of ethylene in liquid carbon dioxide

Yonker, Clement R,Linehan, John C

, p. 249 - 257 (2007/10/03)

In situ, high-pressure NMR was used to investigate the hydroformylation reaction of ethylene in liquid CO2 using Rh(CO)2acac as the catalyst precursor and (p-CF3C6H4)3P, tris(p-trifluoromethylphenyl)phosphine, as the ligand under different thermodynamic conditions (T = 10-23 C, PCO = PH2 = 10-15 bar, PC2H4 = 10-15 bar, PCO2 = 207 bar). 1H-NMR was used to monitor the reaction progress of the hydroformylation of ethylene with a rhodium catalyst under select conditions of temperature and CO2 solvent pressure. Potential resting states of the rhodium catalyst were investigated by 31P(1H)-NMR. This is the first description of a rhodium catalyzed hydroformylation reaction in liquid CO2 monitored in situ by high pressure NMR.

Effect of Ligand Modification on Rhodium-Catalyzed Homogeneous Hydroformylation in Supercritical Carbon Dioxide

Palo, Daniel R.,Erkey, Can

, p. 81 - 86 (2008/10/08)

Several fluoroalkyl- and fluoroalkoxy-substituted tertiary arylphosphines were synthesized and investigated in the homogeneous catalytic hydroformylation of 1-octene using HRh-(CO)L3 (L = tertiary arylphosphine). The activity of the rhodium complex (formed in situ from Rh(CO)2(acac) and L) increased with decreasing basicity of the phosphine according to the series [3,5-(CF3)2C6H3]3P > [4-CF3C6H4]3P ≈ [3-CF3C6H4]3P > [4-CF3C6H4]3P > [4-F(CF2)4(CH2)3C6H 4]3P. The very weakly basic phosphine (C6F5)3P did not complex with Rh(CO)2(acac), most likely due to a combination of electronic and steric factors. Steric effects did not play a role in either the activity or selectivity of the rhodium catalysts that were formed under hydroformylation conditions.

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