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1523213-72-0

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1523213-72-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1523213-72-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,2,3,2,1 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1523213-72:
(9*1)+(8*5)+(7*2)+(6*3)+(5*2)+(4*1)+(3*3)+(2*7)+(1*2)=120
120 % 10 = 0
So 1523213-72-0 is a valid CAS Registry Number.

1523213-72-0Downstream Products

1523213-72-0Relevant academic research and scientific papers

Ruthenium catalyzed selective hydrosilylation of aldehydes

Chatterjee, Basujit,Gunanathan, Chidambaram

supporting information, p. 888 - 890 (2014/01/06)

A chemoselective hydrosilylation method for aldehydes is developed using a ruthenium catalyst [(Ru(p-cymene)Cl2)2] and triethylsilane; a mono hydride bridged dinuclear complex [{(η6-p- cymene)RuCl}2(μ-H-μ-Cl)] a

Preparation and hydrosilylation activity of a molybdenum carbonyl complex that features a pentadentate bis(imino)pyridine ligand

Pal, Raja,Groy, Thomas L.,Bowman, Amanda C.,Trovitch, Ryan J.

supporting information, p. 9357 - 9365 (2014/11/12)

Attempts to prepare low-valent molybdenum complexes that feature a pentadentate 2,6-bis(imino)pyridine (or pyridine diimine, PDI) chelate allowed for the isolation of two different products. Refluxing Mo(CO)6 with the pyridine-substituted PDI ligand, PyEtPDI, resulted in carbonyl ligand substitution and formation of the respective bis(ligand) compound ( PyEtPDI)2Mo (1). This complex was investigated by single-crystal X-ray diffraction, and density functional theory calculations indicated that 1 possesses a Mo(0) center that back-bonds into the π-orbitals of the unreduced PDI ligands. Heating an equimolar solution of Mo(CO) 6 and the phosphine-substituted PDI ligand, Ph2PPrPDI, to 120 °C allowed for the preparation of (Ph2PPrPDI)Mo(CO) (2), which is supported by a κ5-N,N,N,P,P-Ph2PPrPDI chelate. Notably, 1 and 2 have been found to catalyze the hydrosilylation of benzaldehyde at 90°C, and the optimization of 2-catalyzed aldehyde hydrosilylation at this temperature afforded turnover frequencies of up to 330 h-1. Considering additional experimental observations, the potential mechanism of 2-mediated carbonyl hydrosilylation is discussed.

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