301176-96-5 Usage
Uses
Used in Pharmaceutical Industry:
(5-(3-trifluoromethyl)phenyl)furanyl-2-carbaldehyde (E)-thiosemicarbazone is used as a potential pharmaceutical candidate for various applications due to its structural features and potential biological activity. Thiosemicarbazones, in general, have been studied for their anticancer, antiviral, and antimicrobial properties, suggesting that this specific compound may also possess similar pharmacological effects.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (5-(3-trifluoromethyl)phenyl)furanyl-2-carbaldehyde (E)-thiosemicarbazone is used as a subject of study to explore its potential applications in drug development. Its unique structural features make it an interesting compound for further research into its pharmacological effects and possible uses in treating various diseases.
Used in Drug Development:
(5-(3-trifluoromethyl)phenyl)furanyl-2-carbaldehyde (E)-thiosemicarbazone is utilized in drug development as a compound with potential therapeutic applications. (5-(3-trifluoromethyl)phenyl)furanyl-2-carbaldehyde (E)-thiosemicarbazone's structural characteristics and the known pharmacological properties of thiosemicarbazones make it a promising candidate for the development of new drugs targeting cancer, viral, and microbial infections.
Further research is necessary to fully understand the potential uses and properties of (5-(3-trifluoromethyl)phenyl)furanyl-2-carbaldehyde (E)-thiosemicarbazone, including its efficacy, safety, and optimal application methods in various therapeutic areas.
Check Digit Verification of cas no
The CAS Registry Mumber 301176-96-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,1,1,7 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 301176-96:
(8*3)+(7*0)+(6*1)+(5*1)+(4*7)+(3*6)+(2*9)+(1*6)=105
105 % 10 = 5
So 301176-96-5 is a valid CAS Registry Number.
301176-96-5Relevant academic research and scientific papers
Venkatachalam,Pierens, Gregory K.,Reutens, David C.
, p. 98 - 105 (2014)
Thiosemicarbazones possessing electron-donating and electron-withdrawing groups were prepared, and their spectral characteristics determined. In all cases, the spectra showed that one isomer was formed, allowing further functionalization to molecules of biological interest. We provide NMR data for some of the thiosemicarbazones and semicarbazones. We also provide evidence that for 2-pyridyl thiosemicarbazone, the syn isomer slowly converts into the anti isomer in dimethyl sulfoxide solvent with first-order kinetics. Molecular modeling and density functional theory calculations confirmed these observations. Copyright
