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1,3-ditert-butyl-5-nitrobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38896-15-0

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38896-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38896-15-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,8,9 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 38896-15:
(7*3)+(6*8)+(5*8)+(4*9)+(3*6)+(2*1)+(1*5)=170
170 % 10 = 0
So 38896-15-0 is a valid CAS Registry Number.

38896-15-0Downstream Products

38896-15-0Relevant academic research and scientific papers

Regular Two-Dimensional Arrays of Surface-Mounted Molecular Switches: Switching Monitored by UV-vis and NMR Spectroscopy

Santos Hurtado, Carina,Bastien, Guillaume,Ma?át, Milan,?to?ek, Jakub Radek,Dra?ínsky, Martin,Ron?evi?, Igor,Císa?ová, Ivana,Rogers, Charles T.,Kaleta, Ji?í

, p. 9337 - 9351 (2020/06/27)

Using solid-state 15N NMR spectroscopy, the cis/trans isomerization in a two-dimensional (2-D) array of surface-mounted azobenzene-based switches was detected for the first time. In order to achieve this, a new class of rod-shaped molecular switches, suit

Cobalt schiff base complex-catalyzed oxidation of anilines with tert-butyl hydroperoxide

Foerster, Stefan,Rieker, Anton,Maruyama, Kazushige,Murata, Kunihiko,Nishinaga, Akira

, p. 3320 - 3326 (2007/10/03)

Cobalt Schiff base complexes [Co(SB)] catalyze the oxidation of anilines (1) with tert-butyl hydroperoxide to give nitrobenzenes 2 and 4-(tert-butylperoxy)-2,5-cyclohexadien-1-imine derivatives 3 in yield distributions depending on the substitution mode of the substrate. 4-Alkyl- and 4-aryl-2,6-di-tert-butylanilines gave mixtures of 2 and 3, where the higher the bulkiness of the 4-substituent, the higher the yield of 2. With 2,4,6-trimethylaniline, the ratio of oxidations of the nitrogen and C-4 atoms was almost the same; but a hydrolyzed product 5 of the imine was obtained. 2,4,6-Triphenylaniline gave only 2. Nitrobenzene derivatives were also obtained from 2,6-dialkylanilines and 4-substituted anilines. The catalytic activity of Co(SB) depended on the nature of the SB ligand: the formal potential E° and steric factors seem to affect the reaction rate. Kinetic studies showed that the key step may involve hydrogen abstraction from the aniline, presumably by t-BuO? generated from homolytic decomposition of initially formed CoIII(SB)(OO-t-Bu). A precursor of 2 was found to be the nitrosobenzene derivative.

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