26178-94-9 Usage
Uses
Used in Pharmaceutical Industry:
(4Z)-3-methyl-4-[(4-methylphenyl)hydrazono]-5-oxo-4,5-dihydro-1H-pyrazole-1-carbothioamide is used as a potential pharmaceutical compound for its structural features that may contribute to biological activity. The presence of the pyrazole ring and thioamide group, along with the hydrazone functionality, makes it a candidate for the development of new drugs targeting various diseases.
Used in Chemical Synthesis:
In the field of chemical synthesis, (4Z)-3-methyl-4-[(4-methylphenyl)hydrazono]-5-oxo-4,5-dihydro-1H-pyrazole-1-carbothioamide can be used as a precursor for the creation of other compounds. The reactivity of the hydrazone group allows for further chemical modifications, potentially leading to the development of novel molecules with specific applications in various industries.
Used in Drug Discovery:
(4Z)-3-methyl-4-[(4-methylphenyl)hydrazono]-5-oxo-4,5-dihydro-1H-pyrazole-1-carbothioamide is used as a starting point in drug discovery due to its unique structural elements. (4Z)-3-methyl-4-[(4-methylphenyl)hydrazono]-5-oxo-4,5-dihydro-1H-pyrazole-1-carbothioamide's properties make it a valuable tool for researchers to explore its potential in creating new therapeutic agents for various medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 26178-94-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,7 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 26178-94:
(7*2)+(6*6)+(5*1)+(4*7)+(3*8)+(2*9)+(1*4)=129
129 % 10 = 9
So 26178-94-9 is a valid CAS Registry Number.
26178-94-9Relevant academic research and scientific papers
Synthesis and antibacterial activity of some novel 4-aryl hydrazono-2,5-disubstituted-2,4-dihydro-3H-pyrazol-3-ones
Singh, Vipin Kumar
, p. 429 - 432 (2019/01/21)
4-Aryl hydrazono-2,4-dihydro-3H-pyrazol-2,5-disubstituted-3-ones were prepared by the reaction of ethyl-2-arylhydrazono-3-oxybutyrates with substituted hydrazines in the presence of glacial acetic acid at reflux temp. The synthesized compounds have been c
