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(2-methyl-2-((phenylthio)methyl)propane-1,3-diyl)bis(phenylsulfane) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

303148-41-6

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303148-41-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 303148-41-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,3,1,4 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 303148-41:
(8*3)+(7*0)+(6*3)+(5*1)+(4*4)+(3*8)+(2*4)+(1*1)=96
96 % 10 = 6
So 303148-41-6 is a valid CAS Registry Number.

303148-41-6Relevant academic research and scientific papers

Synthesis of C3- and C2-symmetric tris- and bis-sulfoxide ligands by asymmetric oxidation

Dornan, Peter K.,Leung, Priscilla L.,Dong, Vy M.

, p. 4378 - 4384 (2011)

A series of tris- and bis-sulfoxides were synthesized by multiple asymmetric oxidation of the corresponding sulfides. High enantioselectivities were obtained based on Horeau-type amplification of selectivity. Naphthyl-substituted sulfoxides allowed for higher selectivity and greater ease of purification. These sulfoxides were tested as ligands in rhodium-catalyzed olefin hydroacylation and 1,4-addition of phenyl boronic acid to 2-cyclohexen-1-one. While no enantioinduction was observed in hydroacylation, up to 80% ee was obtained for a tris-sulfoxide and a bis-sulfoxide ligand in the 1,4-addition. Bis-sulfoxides with flexible backbones gave lower and inversed enantioselectivity, suggesting backbone rigidity plays a key role in enantioinduction.

Spectroscopic and reactivity differences in metal complexes derived from sulfur containing Triphos homologs

Petuker,Gerschel,Piontek,Ritterskamp,Wittkamp,Iffland,Miller,Van Gastel,Apfel

, p. 13251 - 13262 (2017/10/16)

Herein, we report a simplified method for the synthesis of Triphos homologs H3CC(CH2X)n(CH2Y)3-n (X = SPh, Y = PPh2, n = 0-3). The multidentate compounds were tested for their potential to coordinate metals such as Ni, Fe, and Mo under the same experimental conditions. Cyclic voltammetry, spectroelectrochemical IR investigations as well as DFT calculations were used to examine the electronic alterations in a series of [{H3CC(CH2X)n(CH2Y)3-n}Mo(CO)3] complexes and to evaluate their potential to open coordination sites or to release CO upon oxidation or in the presence of different solvents. In addition, we demonstrate that the catalytic hydrosilylation of N,N-dimethylbenzamide to N,N-dimethylbenzylamine is influenced by the applied tripodal ligand. Our investigations show the high potential of such manipulations to selectively alter the dynamics of the binding properties of Triphos-metal complexes and their reactivity.

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