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thiophene-2-carboxaldehyde-N(4)-(4-nitrophenyl)-thiosemicarbazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31397-20-3

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31397-20-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31397-20-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,3,9 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 31397-20:
(7*3)+(6*1)+(5*3)+(4*9)+(3*7)+(2*2)+(1*0)=103
103 % 10 = 3
So 31397-20-3 is a valid CAS Registry Number.

31397-20-3Downstream Products

31397-20-3Relevant academic research and scientific papers

Synthesis of Cyclic Azomethine Imines by Cycloaddition Reactions of N-Isocyanates and N-Isothiocyanates

Bongers, Amanda,Ranasinghe, Indee,Lemire, Philippe,Perozzo, Alyssa,Vincent-Rocan, Jean-Fran?ois,Beauchemin, André M.

supporting information, p. 3778 - 3781 (2016/08/16)

Various nitrogen-substituted iso(thio)cyanates engage in [3 + 2]-cycloaddition reactions to form azomethine imines containing triazolone, triazole-thione, and pyrazole-thione cores. First, iminoisothiocyanates are shown to undergo aminothiocarbonylation reactions with strained alkenes, and a comparison with recently reported reactions of iminoisocyanates highlights their reduced reactivity. In contrast, amino(thio)carbonylation reactions of imines with iminoisocyanates and iminoisothiocyanates proved more efficient, providing access to triazolone and triazole-thione cores. The dipole products can be converted to valuable heterocyclic cores through simple derivatization reactions.

Novel platinum(II) and palladium(II) complexes of thiosemicarbazones derived from 5-substitutedthiophene-2-carboxaldehydes and their antiviral and cytotoxic activities

Karakü?ük-Iyido?an, Ay?egül,Ta?demir, Demet,Oru?-Emre, Emine El?in,Balzarini, Jan

, p. 5616 - 5624 (2012/01/03)

A series of thiosemicarbazones and their platinum(II) and palladium(II) complexes have been synthesized. The chemical structures of ligands and their complexes were characterized by UV-Vis, IR, 1H NMR, 13C NMR, MS spectra, elemental analysis and TGA. The antiviral and cytotoxic activities of all compounds have been tested. Results of broad antiviral evaluation showed that none of the compounds evaluated endowed with anti-DNA or -RNA virus activity at subtoxic concentrations except for the palladium complex 1b. This compound exhibited slightly selective inhibition against cytomegalovirus. The platinum complex 4a exhibited the best cytostatic activities against human cervix carcinoma. Ligands 2, 4 and 5 showed cytostatic potential. The palladium complexes were in general less cytostatic than the corresponding platinum complexes or unliganded congeners.

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