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5-(3-pyridyl)-10,15,20-tri-p-tolylporphyrin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57412-10-9

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57412-10-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57412-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,4,1 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 57412-10:
(7*5)+(6*7)+(5*4)+(4*1)+(3*2)+(2*1)+(1*0)=109
109 % 10 = 9
So 57412-10-9 is a valid CAS Registry Number.

57412-10-9Downstream Products

57412-10-9Relevant academic research and scientific papers

Synthesis and properties of 5-(3-pyridyl)porphyrinatoruthenium(II) tetramers

Funatsu, Kenji,Yasuda, Naomi,Ichimura, Akio,Santo, Ryoko,Sasaki, Yoichi,Imamura, Taira

experimental part, p. 1556 - 1562 (2009/06/28)

5-(3-Pyridyl)porphyrinatoruthenium(II) tetramers, [{Ru(3-PyT 3porph)(CO)}4] (1), [{Ru(3-PytB3porph)(CO)} 4] (2), [{Ru(3-PyHex3porph)(CO)}4] (3), and [{Ru(3-PytB3porph)(py)}4] (4) were prepared. The structures of the isolated tetramers were determined to be rhombic shaped with two chemically nonequivalent porphyrinatoruthenium(II) subunits by 1HNMR, IR, and ESI-MS measurements. The tetramers were stable in benzene at 70 °C. However, the tetramers reacted with a large excess of pyridine to give two geometrical isomers of porphyrinatoruthenium(II) in dichloromethane at room temperature as observed by 1H NMR spectrometry. U V-vis spectra of the tetramers showed splitting or broadening of the Soret band due to excitonic interactions. Stepwise oxidations of the porphyrin rings or the ruthenium ions in the cyclic tetramer skeleton were observed in cyclic voltammograms.

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