6293-75-0 Usage
Uses
Used in Pharmaceutical Research:
(2E)-2-[2-(7,8-dimethyl-2,4-dioxo-3,4-dihydrobenzo[g]pteridin-10(2H)-yl)ethylidene]hydrazinecarbothioamide is used as a research compound for exploring its potential biological activities and applications in the development of new drugs and therapies.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2E)-2-[2-(7,8-dimethyl-2,4-dioxo-3,4-dihydrobenzo[g]pteridin-10(2H)-yl)ethylidene]hydrazinecarbothioamide is used as a starting material or a building block for the synthesis of more complex molecules with potential therapeutic properties.
Note: Since the provided materials do not specify any particular application industry or reason for the use of (2E)-2-[2-(7,8-dimethyl-2,4-dioxo-3,4-dihydrobenzo[g]pteridin-10(2H)-yl)ethylidene]hydrazinecarbothioamide, the uses listed above are general and based on the potential of the compound as described in the materials. Further research and development may reveal more specific applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 6293-75-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6293-75:
(6*6)+(5*2)+(4*9)+(3*3)+(2*7)+(1*5)=110
110 % 10 = 0
So 6293-75-0 is a valid CAS Registry Number.
6293-75-0Relevant academic research and scientific papers
Synthesis, structure and photophysical properties of a flavin-based platinum(ii) complex
Kobayashi, Atsushi,Ohbayashi, Korin,Aoki, Rie,Chang, Ho-Chol,Kato, Masako
experimental part, p. 3484 - 3489 (2011/07/30)
We synthesized a thiosemicarbazone-functionalized flavin (Fl-(H)TSC: 2-[2-(3,4-dihydro-7,8-dimethyl-2,4-dioxobenzo[g]pteridin-10(2H)-yl)ethylidene] -hydrazinecarbothioamide) and its Pt(ii) complex [Pt(Fl-TSC)2], and characterized it using X-ray diffraction, UV-visible absorption and luminescence spectroscopy. X-ray structural analysis for [Pt(Fl-TSC)2] revealed that the structure of the isoalloxazine part was almost the same as that in lumiflavin (7,8,10-trimethylisoalloxazine), and the thiosemicarbazone moiety acted as a bidentate ligand to form a PtS2N2 planar conformation. UV-visible absorption and luminescence spectra of these compounds were very similar to those of riboflavin, but the emission intensity and the lifetime decreased considerably. Theoretical calculations suggested that the charge-separated state (Fl--TSC+) contributed to the faster quenching from the 1π-π* emission state. The Royal Society of Chemistry 2011.
