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1-(3-chlorophenyl)-3-(4-fluorophenyl)thiourea is an organic compound with the chemical formula C12H9ClFN2S. It is a derivative of thiourea, featuring a 3-chlorophenyl group at the 1-position and a 4-fluorophenyl group at the 3-position. 1-(3-chlorophenyl)-3-(4-fluorophenyl)thiourea is characterized by its unique structure, which combines a chlorine atom and a fluorine atom on different aromatic rings, potentially influencing its chemical properties and reactivity. It is a white crystalline solid and is used in various chemical research and industrial applications, such as the synthesis of pharmaceuticals and agrochemicals. Due to its specific functional groups, it may exhibit different chemical behaviors compared to other thiourea derivatives, making it a subject of interest in the field of organic chemistry.

370-18-3

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370-18-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 370-18-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 370-18:
(5*3)+(4*7)+(3*0)+(2*1)+(1*8)=53
53 % 10 = 3
So 370-18-3 is a valid CAS Registry Number.

370-18-3Downstream Products

370-18-3Relevant academic research and scientific papers

Synthesis and in vitro urease inhibitory activity of N,N′- disubstituted thioureas

Khan, Khalid Mohammed,Naz, Farzana,Taha, Muhammad,Khan, Ajmal,Perveen, Shahnaz,Choudhary,Voelter, Wolfgang

, p. 314 - 323 (2014/02/14)

Thiourea derivatives (1-38) were synthesized and evaluated for their urease inhibition potential. The synthetic compounds showed a varying degree of in vitro urease inhibition with IC50 values 5.53 ± 0.02-91.50 ± 0.08 μM, most of which are superior to the standard thiourea (IC50 = 21.00 ± 0.11 μM). In order to ensure the mode of inhibition of these compounds, the kinetic study of the most active compounds has been carried out. Most of these inhibitors were found to be mixed-type of inhibitors, except compounds 13 and 30 which were competitive, while compound 19 was identified as non-competitive inhibitor with Ki values between 8.6 and 19.29 μM.

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