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O-phenyl cyclohexylcarbamothioate is a chemical compound with the molecular formula C13H17NOS. It is an organic compound that belongs to the class of carbamothioates, which are derivatives of carbamic acid. o-phenyl cyclohexylcarbamothioate is characterized by the presence of a cyclohexyl group attached to a phenyl ring through a carbamothioate linkage. It is used in various applications, including as an intermediate in the synthesis of pharmaceuticals and agrochemicals, due to its potential to form stable derivatives with biological activity. The compound's structure and properties make it a versatile building block in organic synthesis, particularly in the development of compounds with specific therapeutic or pesticidal properties.

2423-27-0

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2423-27-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2423-27-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,2 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2423-27:
(6*2)+(5*4)+(4*2)+(3*3)+(2*2)+(1*7)=60
60 % 10 = 0
So 2423-27-0 is a valid CAS Registry Number.

2423-27-0Relevant academic research and scientific papers

Synthesis of isothiocyanates by reaction of amines with phenyl chlorothionoformate via one-pot or two-step process

Li, Zheng-Yi,Ma, Hong-Zhao,Han, Chen,Xi, Hai-Tao,Meng, Qi,Chen, Xin,Sun, Xiao-Qiang

, p. 1667 - 1674 (2013/07/19)

A facile and efficient synthesis of isothiocyanates from amines is described. This method involves the reaction of amines with phenyl chlorothionoformate in the presence of solid sodium hydroxide by either a one-pot process or a two-step approach. The one-pot process is useful for preparing alkyl and electron-rich aryl isothiocyanates, whereas the two-step approach is more versatile, working very well not only for alkyl and electron-rich aryl isothiocyanates, but also for highly electron-deficient aryl and heterocyclic isothiocyanates. Georg Thieme Verlag Stuttgart, New York.

AMINO QUINOLINE DERIVATIVES INHIBITORS OF HCV

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Page/Page column 115, (2013/07/05)

A compound of Formula I: or a pharmaceutically acceptable salt thereof, wherein the substituents are defined herein, and methods of treating HCV infection in a patient are disclosed.

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