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N-butyl-4-trifluoromethylbenzene-1,2-diamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

320406-61-9

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320406-61-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 320406-61-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,0,4,0 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 320406-61:
(8*3)+(7*2)+(6*0)+(5*4)+(4*0)+(3*6)+(2*6)+(1*1)=89
89 % 10 = 9
So 320406-61-9 is a valid CAS Registry Number.

320406-61-9Relevant academic research and scientific papers

Tuning Flavin-Based Photocatalytic Systems for Application in the Mild Chemoselective Aerobic Oxidation of Benzylic Substrates

Tolba, Amal Hassan,Vávra, Franti?ek,Chudoba, Josef,Cibulka, Radek

, p. 1579 - 1585 (2020)

New flavin-based photocatalytic systems used for chemoselective aerobic visible-light oxidations have been developed by tuning the flavin structure and reaction conditions. 1,3-Dimethyl-7-trifluoromethylalloxazine (2) and 10-butyl-3-methyl-7-trifluoromethylisoalloxazine (3) were shown to mediate the selective oxidation of benzyl alcohols to form aldehydes in the presence of Cs2CO3. Flavin 3 was superior in the oxidation of toluene derivatives to form aldehydes in the presence of trifluoroacetic acid. On the other hand, photooxidations provided by ethylene-bridged quaternary flavinium salt 1 gave the corresponding carboxylic acids. The usefulness of the developed catalytic systems using 1–3 was also demonstrated in the oxidation of secondary benzylic and aliphatic alcohols, and benzylic methylene groups to form the corresponding ketones. The systems have the advantage of a broad substrate scope and metal-free conditions, which distinguish them from the previously reported flavin photooxidation reactions.

Imidazopyridinone derivatives and their use as phosphodiesterase inhibitors

-

, (2008/06/13)

A compound (Ia): wherein the variables are defined in the specification, its prodrug or a pharmaceutically acceptable salt thereof useful in the treatment of angina, hypertension etc.

Synthesis and antimicrobial activity of some new 2-phenyl-N-substituted carboxamido-1H-benzimidazole derivatives

Goeker, Hakan,Tuncbilek, Meral,Suezen, Sibel,Kus, Canan,Altanlar, Nurten

, p. 148 - 152 (2007/10/03)

Some 1H-benzimidazole-carboxamide derivatives were prepared and their antimicrobial activities against Staphyloccus aureus, Escherichia coli and Candida albicans evaluated. Compounds 18, 22, and 25 exhibited the best activity against Candida albicans.

Design and syntheses of a series of novel serotonin3 antagonists

Hori,Suzuki,Yamamoto,Nakajima,Ozaki,Ohtaka

, p. 1832 - 1841 (2007/10/02)

From a structural comparison study between serotonin and serotonin3 (5- HT3) antagonists using a two-dimensional grid template composed of regular hexagons, we deduced structural modification patterns from agonists to antagonists, an

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