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N-(4-bromo-phenyl)-N'-m-tolyl-thiourea is an organic compound characterized by its unique chemical structure. It is a derivative of thiourea, with a 4-bromophenyl group attached to the nitrogen atom and an m-tolyl group attached to the other nitrogen atom. N-(4-bromo-phenyl)-N'-m-tolyl-thiourea is known for its potential applications in various chemical reactions and synthesis processes, particularly in the field of pharmaceuticals and agrochemicals. Its molecular formula is C14H12BrN2S, and it has a molecular weight of 323.23 g/mol. The presence of the bromine atom and the m-tolyl group gives N-(4-bromo-phenyl)-N'-m-tolyl-thiourea specific properties that can be exploited in various chemical transformations, making it a valuable intermediate in the synthesis of more complex molecules.

22937-95-7

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22937-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22937-95-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,3 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22937-95:
(7*2)+(6*2)+(5*9)+(4*3)+(3*7)+(2*9)+(1*5)=127
127 % 10 = 7
So 22937-95-7 is a valid CAS Registry Number.

22937-95-7Downstream Products

22937-95-7Relevant academic research and scientific papers

A simple and straightforward synthesis of phenyl isothiocyanates, symmetrical and unsymmetrical thioureas under ball milling

Zhang, Ze,Wu, Hao-Hao,Tan, Ya-Jun

, p. 16940 - 16944 (2013/09/24)

Promoted by KOH under ball milling, anilines were efficiently transformed into isothiocyanates (in presence of 5.0 equiv. CS2) or symmetrical thioureas (in presence of 1.0 equiv. CS2), without using any other harsh or toxic decomposition reagent. Some in situ generated isothiocyanates can directly "click" with other amines to afford unsymmetrical thioureas.

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