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213881-38-0

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213881-38-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 213881-38-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,8,8 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 213881-38:
(8*2)+(7*1)+(6*3)+(5*8)+(4*8)+(3*1)+(2*3)+(1*8)=130
130 % 10 = 0
So 213881-38-0 is a valid CAS Registry Number.

213881-38-0Relevant articles and documents

Reaction of 8-arenesulfonyloxy-2-methylquinolines with 4,6-di(tert-butyl)-3-nitro-1,2-benzoquinone

Mikhailov,Kolodina,Artyushkina,Dushenko,Sayapin,Minkin

, p. 595 - 598 (2015)

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COMPOUND, COLOR MATERIAL COMPOSITION CONTAINING THE SAME, AND RESIN COMPOSITION CONTAINING THE SAME

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Paragraph 0171-0173, (2017/07/13)

PROBLEM TO BE SOLVED: To provide a novel compound, a color material composition containing the same and a resin composition containing the same that improve the color purity, luminance and contrast ratio in color filter production employing a pigment dispersion method using pigments. SOLUTION: The invention provides a compound represented by the chemical formula 1, a color material composition containing the same, and a resin composition containing the same. (Y is a direct bond or CQ1Q2; R1-R14, Q1 and Q2 are each independently H, D, or a halogen group, nitrile group, nitro group, hydroxy group, carbonyl group, ester group, imide group, amide group, carboxy group (-COOH), or -OC(=O)R'''; and the like.) SELECTED DRAWING: Figure 1 COPYRIGHT: (C)2017,JPOandINPIT

Photochemical cleavage reactions of 8-quinolinyl sulfonates in aqueous solution

Kageyama, Yoshiyuki,Ohshima, Ryosuke,Sakurama, Kazusa,Fujiwara, Yoshihisa,Tanimoto, Yoshifumi,Yamada, Yasuyuki,Aoki, Shin

experimental part, p. 1257 - 1266 (2010/05/02)

Photochemical cleavage reactions of 8-quinolinyl benzenesulfonate derivatives and related sulfonates in aqueous solutions are reported. The 8-quinolinyl benzenesulfonates undergo photolysis upon photoirradiation at 300-330 nm to give the corresponding 8-quinolinols and benzenesulfonic acids with the production of only negligible amounts of byproducts. The effects of substituent groups of the 8-quinolinyl moiety and the benzene ring on the photolysis reactions were examined. Based on steady-state mechanistic studies using a triplet sensitizer, a triplet quencher, and electron donors, it was suggested that the photolysis proceeds mainly via the homolytic cleavage of S-O bonds in the excited triplet state.

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