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Benzoic acid, 4-nitro-, 2-[[(4-fluorophenyl)amino]thioxomethyl]hydrazide is a complex organic compound with the chemical formula C14H11FN4O3S. It is a derivative of benzoic acid, featuring a nitro group at the 4-position and a hydrazide group at the 2-position. The hydrazide is connected to a thioxomethyl group, which in turn is linked to a 4-fluorophenyl ring through an amino group. Benzoic acid, 4-nitro-, 2-[[(4-fluorophenyl)amino]thioxomethyl]hydrazide is characterized by its molecular structure, which includes a benzene ring with a carboxyl group, a nitro group, and a hydrazide group attached to a sulfur-containing moiety. It is important to note that the compound's specific properties, such as solubility, stability, and reactivity, are influenced by the presence of these functional groups. The compound may have potential applications in the fields of pharmaceuticals or chemical research, but further information on its specific uses or properties would be required to provide a more detailed analysis.

403-35-0

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403-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 403-35-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,0 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 403-35:
(5*4)+(4*0)+(3*3)+(2*3)+(1*5)=40
40 % 10 = 0
So 403-35-0 is a valid CAS Registry Number.

403-35-0Downstream Products

403-35-0Relevant academic research and scientific papers

1,3,4-Thiadiazole derivatives. Synthesis, structure elucidation, and structure-antituberculosis activity relationship investigation

Oru?, El?in E.,Rollas, Sevim,Kandemirli, Fatma,Shvets, Nathaly,Dimoglo, Anatholy S.

, p. 6760 - 6767 (2007/10/03)

A series of 2,5-disubstituted-1,3,4-thiadiazoles were synthesized, the compounds structures were elucidated and screened for the antituberculosis activity against Mycobacterium tuberculosis H37Rv using the BACTEC 460 radiometric system. Among the tested compounds, 2-phenylamino-5-(4-fluorophenyl) -1,3,4-thiadiazole 22 showed the highest inhibitory activity. The relationships between the structures of compounds and their antituberculosis activity were investigated by the Electronic-Topological Method (ETM) and feed forward neural networks (FFNNs) trained with the back-propagation algorithm. As a result of the approach, a system of pharmacophores and anti-pharmacophores has been found that effectively separates compounds of the examination set into groups of active and inactive compounds. The system can be applied to the screening and design of new active compounds possessing skeletons similar to those used in the present study.

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