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2-deuterio-2-(4-nitrophenyl)-1,3-dithiane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35531-59-0

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35531-59-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35531-59-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,5,3 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 35531-59:
(7*3)+(6*5)+(5*5)+(4*3)+(3*1)+(2*5)+(1*9)=110
110 % 10 = 0
So 35531-59-0 is a valid CAS Registry Number.

35531-59-0Relevant academic research and scientific papers

Mechanism of the Water-Catalyzed Photoisomerization of p-Nitrobenzaldehyde

Wubbels, Gene G.,Kalhorn, Thomas F.,Johnson, Douglas E.,Campbell, Dana

, p. 4664 - 4670 (1982)

p-Nitrobenzaldehyde is observed to photoisomerize cleanly to p-nitrobenzoic acid in aqueous solutions but to be photostable in pure acetonitrile or acetic acid.The dimethyl acetal of p-nitrobenzaldehyde is photostable in water.The quantum yield (0.034 at

Nitration and Oxidation of Substituted Benzaldehydes in Solutions of Dinitrogen Pentaoxide or Nitronium Trifluoromethanesulfonate in Nitric Acid

Moodie, Roy B.,Willmer, Richard

, p. 229 - 234 (2007/10/02)

The competition between oxidation to the corresponding benzoic acid and nitration in the aromatic ring of some substituted benzaldehydes has been probed by kinetic and product studies.Nitrodeformylation was not detected. 4-Carboxybenzaldehyde is nitrated

1,3-Dithienium- and 1,3-Dithiolenium Salts, IV. 1,3-Dithian-2-ylium Tetrafluoroborates - New Agents for the Synthesis of 1-Deuterioaldehydes

Stahl, Ingfried

, p. 3166 - 3171 (2007/10/02)

The 1,3-dithian-2-ylium tetrafluoroborates 3 react in good yields with sodium borohydride (4) to give the 1,3-dithianes 6 and with sodium borodeuteride (5) to form the precursors 7 of 1-deuterated aldehydes 8.Three 1-deuterioaldehydes 8 are synthesized exemplarily by dethioacetalization of 7.

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