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1-(4-chlorophenyl)-3-(4-nitrophenyl)-1H-pyrazole-5(4H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60798-18-7

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60798-18-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60798-18-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,9 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 60798-18:
(7*6)+(6*0)+(5*7)+(4*9)+(3*8)+(2*1)+(1*8)=147
147 % 10 = 7
So 60798-18-7 is a valid CAS Registry Number.

60798-18-7Downstream Products

60798-18-7Relevant academic research and scientific papers

Synthesis and cytotoxic evaluation of some substituted 5-pyrazolones and their urea derivatives

Erturk, Aliye Gediz,Omerustaoglu, Hilal

, (2020)

In this paper, a series of new substituted-5-pyrazolones were first synthesized, then formulated by the Vilsmeier–Haack reaction to obtain substituted-4-carbaldehyde-5-pyrazolones. In the final step, when urea was reacted with formulated pyrazolones, we found that, instead of the C=N bond in azomethine form, the compounds tautomerized to form a series of novel pyrazole-4ylidenemethylurea structures. The structures of these compounds were elucidated by FTIR, 1H, 13C NMR, LC-MS/MS, and elemental analysis methods. The cytotoxic and antioxidant effects of substituted 5-pyrazolones and their pyrazolone-urea derivatives were investigated in metastatic A431 and noncancerous HaCaT human keratinocytes by a mitochondrial activity test. The effects of the compounds on the migration of cancerous and noncancerous cell lines were investigated by using a cell scratch assay. The General Linear Model, Statistical Package for Social Sciences (SPSS v26) was used to determine if there was a statistically significant difference between the control and the treatment groups. Four of the nine compounds showed an antioxidant effect. All 5-pyrazolone-urea compounds showed higher toxicity (p 0.05) in cancerous A431 cells compared to noncancerous cells at all time points. All compounds also showed a biphasic hormetic effect. Four of the nine compounds inhibited cell migration.

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