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[3-(3-Bromo-phenyl)-thioureido]-acetic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111633-99-9

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111633-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111633-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,6,3 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 111633-99:
(8*1)+(7*1)+(6*1)+(5*6)+(4*3)+(3*3)+(2*9)+(1*9)=99
99 % 10 = 9
So 111633-99-9 is a valid CAS Registry Number.

111633-99-9Downstream Products

111633-99-9Relevant academic research and scientific papers

Novel Copper-Containing Cytotoxic Agents Based on 2-Thioxoimidazolones

Krasnovskaya, Olga O.,Guk, Dmitry A.,Naumov, Alexey E.,Nikitina, Vita N.,Semkina, Alevtina S.,Vlasova, Kseniya Yu.,Pokrovsky, Vadim,Ryabaya, Oksana O.,Karshieva, Saida S.,Skvortsov, Dmitry A.,Zhirkina, Irina V.,Shafikov, Radik R.,Gorelkin, Petr V.,Vaneev, Alexander N.,Erofeev, Alexander S.,Mazur, Dmitrii M.,Tafeenko, Viktor A.,Pergushov, Vladimir I.,Melnikov, Mikhail Ya.,Soldatov, Mikhail A.,Shapovalov, Victor V.,Soldatov, Alexander V.,Akasov, Roman. A.,Gerasimov, Vasily M.,Sakharov, Dmitry A.,Moiseeva, Anna A.,Zyk, Nikolay V.,Beloglazkina, Elena K.,Majouga, Alexander G.

, p. 13031 - 13063 (2020/12/17)

A series of 73 ligands and 73 of their Cu+2 and Cu+1 copper complexes with different geometries, oxidation states of the metal, and redox activities were synthesized and characterized. The aim of the study was to establish the structure-activity relations

MECHANISM OF BASE-CATALYZED CYCLIZATION OF ETHYL N-(SUBSTITUTED AMINOCARBONYL)GLYCINATES

Mindl, Jaromir,Sterba, Vojeslav

, p. 156 - 161 (2007/10/02)

The cyclization rate constants have been measured of substituted ethyl N-(phenylaminocarbonyl)-, N-(alkylaminocarbonyl)-, and N-(phenylaminothiocarbonyl)glycinates RNHCXNHCH2CO2C2H5 (X=O,S).Logarithms of these constants increase with decreasing basicity of the amines down to the value of pKa(RNH2) = 5.5.The rate-limiting step of the reaction is formation of the tetrahedral intermediate.With ethyl N-(phenylaminocarbonyl)glycinates (whose pKa(RNH2) values are higher) this dependence, on the contrary, slightly decreases, and the acid-catalyzed splitting off of ethoxy group from the cyclic intermediate becomes rate-li miting.The cyclization rate of a series of ethyl N-(phenylaminothiocarbonyl)glycinates is practically independent of the pKa(RNH2) values, the change in the rate limiting step would take place at pH about 9.

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