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N-Phenylethyl-N'-hydroxyethylthioharnstoff is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29146-59-6

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29146-59-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29146-59-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,1,4 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 29146-59:
(7*2)+(6*9)+(5*1)+(4*4)+(3*6)+(2*5)+(1*9)=126
126 % 10 = 6
So 29146-59-6 is a valid CAS Registry Number.

29146-59-6Relevant academic research and scientific papers

Thiocarbonyl Surrogate via Combination of Sulfur and Chloroform for Thiocarbamide and Oxazolidinethione Construction

Tan, Wei,Wei, Jianpeng,Jiang, Xuefeng

supporting information, p. 2166 - 2169 (2017/04/27)

An efficient and practical thiocarbonyl surrogate via combination of sulfur and chloroform has been developed. A variety of thiocarbamides and oxazolidinethiones have been established, including chiral thiourea catalysts and chiral oxazolidinethione auxiliaries with high selectivity. Meanwhile, pesticides Diafenthiuron (an acaricide), ANTU (a rodenticide), and Chloromethiuron (an insecticide) were practically synthesized through this method in gram scale. Dicholorocarbene, as the key intermediate, was further confirmed via a carbene-trapping control experiment.

Aminothiazines et aminothiazoles analogues ouverts du levamisole: synthese et approche du mode d'action nematicide

Caujolle, Raymond,Amarouch, Hamid,Payard, Marc,Loiseau, Philippe R.,Bories, Christian,et al.

, p. 287 - 292 (2007/10/02)

New compounds with thiazoline or dihydrothiazine rings substituted by alkylamino or arylamino groups were synthesized and screened in vitro against three Nematodes.Inhibition of fumarate-reductase activity was also evaluated.For all in vitro anti-parasitic tests, dihydrothiazines were more potent than corresponding thiazolines derivatives, however, thiazolines showed a greater inhibition of fumarate-reductase.

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