21198-80-1 Usage
Description
[amino(1-methylethylidene)carbonohydrazonoyl]selanyl, a selenoamide compound with the molecular formula C4H11N3OSe, is derived from the amino acid proline and contains selenium. This chemical compound is of interest in the fields of medicinal chemistry and biochemistry due to its potential applications in the development of pharmaceuticals and bioactive compounds. As a selenoamide, it may possess antioxidant properties and could be involved in biological processes that require selenium.
Uses
Used in Pharmaceutical Development:
[amino(1-methylethylidene)carbonohydrazonoyl]selanyl is used as a key compound in the development of pharmaceuticals for its potential antioxidant properties and its role in biological processes involving selenium. Its specific chemical and biological properties make it a valuable candidate for further study and application in the creation of new drugs and therapies.
Used in Bioactive Compound Synthesis:
In the field of organic synthesis, [amino(1-methylethylidene)carbonohydrazonoyl]selanyl serves as an important building block for the synthesis of bioactive compounds. Its unique structure and selenium content contribute to the development of novel molecules with potential applications in various industries, including healthcare and agriculture.
Used in Chemical Research:
[amino(1-methylethylidene)carbonohydrazonoyl]selanyl is also utilized as a research tool in chemical laboratories. Its properties and reactivity are studied to better understand the behavior of selenoamide compounds and their potential applications in various chemical processes and reactions.
Used in Antioxidant Applications:
Given its potential antioxidant properties, [amino(1-methylethylidene)carbonohydrazonoyl]selanyl may be used as an additive or component in various industries, such as the food and cosmetics industries, to enhance the shelf life and quality of products by neutralizing harmful free radicals.
Used in Environmental Applications:
The antioxidant properties of [amino(1-methylethylidene)carbonohydrazonoyl]selanyl may also find use in environmental applications, such as in the remediation of contaminated sites or the development of eco-friendly materials that can help reduce the impact of human activities on the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 21198-80-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,1,9 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21198-80:
(7*2)+(6*1)+(5*1)+(4*9)+(3*8)+(2*8)+(1*0)=101
101 % 10 = 1
So 21198-80-1 is a valid CAS Registry Number.
21198-80-1Relevant articles and documents
Co(III) complexes of (1,3-selenazol-2-yl)hydrazones and their sulphur analogues
Filipovi?, Nenad R.,Elshaflu, Hana,Grubi?i?, Sonja,Jovanovi?, Ljiljana S.,Rodi?, Marko,Novakovi?, Irena,Male?evi?, Aleksandar,Djordjevi?, Ivana S.,Li, Haidong,?oji?, Ne?o,Marinkovi?, Aleksandar,Todorovi?, Tamara R.
supporting information, p. 2910 - 2924 (2017/03/11)
The first Co(iii) complexes with (1,3-selenazol-2-yl)hydrazones as an unexplored class of ligands were prepared and characterized by NMR spectroscopy and X-ray diffraction analysis. The novel ligands act as NNN tridentate chelators forming octahedral Co(iii) complexes. The impact of structural changes on ligands' periphery as well as that of isosteric replacement of sulphur with selenium on the electrochemical and electronic absorption features of complexes are explored. To support the experimental data, density functional theory (DFT) calculations were also conducted. Theoretical NMR chemical shifts, the relative energies and natural bond orbital (NBO) analysis are calculated within the DFT approach, while the singlet excited state energies and HOMO-LUMO energy gap were calculated with time-dependent density functional theory (TD-DFT). The electrophilic f- and nucleophilic f+ Fukui functions are well adapted to find the electrophile and nucleophile centres in the molecules. Both (1,3-selenazol-2-yl)- and (1,3-thiazol-2-yl)hydrazone Co(iii) complexes showed potent antimicrobial and antioxidant activity. A significant difference among them was a smaller cytotoxicity of selenium compounds.
