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trans-9,10-dihydroxy-9,10-diphenyl-9,10-dihydroanthracene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36204-66-7

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36204-66-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36204-66-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,2,0 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36204-66:
(7*3)+(6*6)+(5*2)+(4*0)+(3*4)+(2*6)+(1*6)=97
97 % 10 = 7
So 36204-66-7 is a valid CAS Registry Number.

36204-66-7Relevant academic research and scientific papers

Kinetic studies on the reactions of electrogenerated 9,10-diphenyl-anthracene cation radical with water and alcohols by means of column-electrolytic stopped-flow method

Oyama,Nozaki,Nagaoka,Okazaki

, p. 33 - 41 (2007/10/02)

The reactions of 9,10-diphenylanthracene cation radical (DPA+.) with water and alcohols in acetonitrile (AN) were studied using a novel column-electrolytic stopped-flow spectrophotometric method. The reaction was first-order with respect to DPA+. in all reactions. The reaction orders of other reactants were determined by plotting the logarithms of the apparent first-order rate constants (k(app)'s) against the logarithms of the concentration of reactants. The plot of log k(app) vs. log [alcohols] was linear, and hence the reaction was clearly determined to be second-order. On the other hand, the log k(app) vs. log [water] plot did not show a linear relationship. Similar results were obtained in the reactions of 9,10-dimethylanthracene cation radical with water and methanol. Comparing the results obtained with water and alcohols, and considering the changes in the physicochemical properties of the AN-water medium, it was concluded that the reaction of water was second-order, though it had been believed previously to be first-order. Products of the reactions are trans- and cis-9,10-dialkoxy-9,10-diphenyl-9,10-dihydroanthracene in many cases.

Chemilumineszenz- und Oxidationsreactionen von Phthaloylperoxid und verwandten Verbindungen.

Gundermann, Karl-Dietrich,Steinfatt, Manfred,Witt, Peter,Paetz, Christian,Poeppel, Karl-Ludwig

, p. 2801 - 2822 (2007/10/02)

Phthaloylperoxid (PPO) und 4,5-Dichlorphthaloylperoxid ergeben mit fluoreszenzfaehigen aromatischen Kohlenwasserstoffen wie 9,10-Diphenylanthracen (DPA), 9,10-Bis(phenylethinyl)anthracen, Pyren, Perylen, aber auch heterocyclischen Verbindungen wie 1,3-Diphenylbenzofuran (9), Luminol oder Fluorescein Chemilumineszenz, die Quantenausbeuten bis 1E-3 Einstein/mol erreichen kann, wenn Phthalsaeureester als Loesungsmittel eingesetzt werden.Die Chemilumineszenz wird durch Sauerstoff hinsichtlich der Maximalintensitaet gesteigert, hinsichtlich der Lichtausbeute auf etwa 80percent verringert.Da bei Derivaten des 1,3-Diphenyl-benzofurans sowohl Chemilumineszenz, als auch Bildung der entsprechenden "Photooxdationsprodukte" (bei 9: o-Dibenzoylbenzol) beobachtet wurde, wird die Moeglichkeit der Bildung von Singulett-Sauerstoff aus PPO diskutiert.Die Bildung von Phthalsaeure-halbestern aus PPO und Olefinen anstelle des Auftretens von Hydroperoxiden wird ueber die thermodynamisch moegliche intermediaere Bildung von Benzocyclobutendion erklaert und ist kein grundsaetzlicher Widerspruch gegen das Auftreten von Singulett-Sauerstoff bei PPO-Reaktionen.

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