3540-90-7 Usage
Uses
Used in Organic Synthesis:
(1Z)-1,2-diphenylethane-1,2-dione semicarbazone is used as a reagent in organic synthesis for its ability to detect and quantify certain functional groups in compounds, making it a valuable tool in the development of new chemical entities.
Used in Antiviral Applications:
In the field of virology, (1Z)-1,2-diphenylethane-1,2-dione semicarbazone is used as an antiviral agent, leveraging its potential biological activities to combat viral infections, thereby offering a promising avenue for the development of antiviral therapies.
Used in Antibacterial Applications:
(1Z)-1,2-diphenylethane-1,2-dione semicarbazone is employed as an antibacterial agent, exhibiting properties that can help in the fight against bacterial infections, contributing to the discovery of new antimicrobial agents.
Used in Antifungal Applications:
(1Z)-1,2-diphenylethane-1,2-dione semicarbazone is also used as an antifungal agent, showing promise in controlling fungal infections, which is crucial for both medical and agricultural applications.
Used in Anti-Inflammatory Applications:
(1Z)-1,2-diphenylethane-1,2-dione semicarbazone has been studied for its potential as an anti-inflammatory agent, suggesting that it could be utilized in the treatment of inflammation-related conditions.
Used in Analytical Chemistry:
In the realm of analytical chemistry, (1Z)-1,2-diphenylethane-1,2-dione semicarbazone is used as a chelating agent, which is instrumental in the detection and analysis of metal ions, enhancing the capabilities of analytical techniques.
Used in Pharmaceutical Development:
Given its diverse range of biological activities, (1Z)-1,2-diphenylethane-1,2-dione semicarbazone is a candidate for pharmaceutical development, with potential applications in the creation of new drugs for various therapeutic areas.
Check Digit Verification of cas no
The CAS Registry Mumber 3540-90-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,4 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3540-90:
(6*3)+(5*5)+(4*4)+(3*0)+(2*9)+(1*0)=77
77 % 10 = 7
So 3540-90-7 is a valid CAS Registry Number.
3540-90-7Relevant academic research and scientific papers
Selective access to new semicarbazones and thiosemicarbazones derived from benzil. Study of their conversion reactions
Arquero, Agueda,Canadas, Marta,Martinez-Ripoll, Martin,Mendiola, Ma. Antonia,Rodriguez, Ana
, p. 11271 - 11284 (2007/10/03)
New Schiff bases from benzil with semicarbazide and thiosemicarbazide are reported. An open chain molecule, benzilbissemicarbazone 1 was prepared in presence of lithium hydroxide. A cycle 6-methoxy-1,6-diphenyl-4-thio- 3,4,5,6-tetrahydro-2,3,5-triazine 7 was obtained from thiosemicarbazide. A cyclic molecule, 1,6-diphenyl-4-oxo-3,4,5,6-tetrahydro-2,3,5-triazine 4 was produced from the recrystallization of 3 in chloroform. A new macrocyclic complex 8 was isolated from the open chain 6 in the presence of iron (III) chloride hexahydrated. Compounds 1, 2 convert into the cyclic 3 heated under reflux. In addition, we have got an iron complex 5 of 1 using the compound 2 as precursor. The crystal structure of 7 was obtained by single crystal X- Ray diffraction.
Copper(II) Complexes of Hydrazone Derivatives
Souza, P.,Mendiola, M. A.,Arquero, A.,Fernandez, V.,Gutierrez-Puebla, E.,Ruiz-Valero, C.
, p. 263 - 271 (2007/10/02)
Three benzil based, macrocyclic oxygen-, nitrogen-, and sulfur-containing ligands, (3,4,10,11-tetraphenyl-1,2,5,6,8,9,12,13-octaazacyclotetradeca-7,14-dithione-2,4,9,11-tetraene) ethanol (L1), 10,11-diethoxy-3,4,10,11-tetraphenyl-1,2,5,6,8,9,12
