73236-43-8 Usage
Uses
Used in Pharmaceutical Industry:
5-(2-Propenylthio)-2,4(1H,3H)-pyrimidinedione is used as a potential active pharmaceutical ingredient for the development of new drugs. Its unique structure and potential biological activities make it a promising candidate for the treatment of various diseases, including viral, bacterial, or fungal infections.
Used in Antiviral Applications:
In the field of antiviral research, 5-(2-Propenylthio)-2,4(1H,3H)-pyrimidinedione is used as a potential antiviral agent. Its pyrimidine structure may allow it to interfere with viral replication processes, thereby inhibiting the spread of viruses and reducing the severity of viral infections.
Used in Antibacterial Applications:
5-(2-Propenylthio)-2,4(1H,3H)-pyrimidinedione is also used as a potential antibacterial agent. Its ability to target and disrupt bacterial processes may contribute to the development of new antibiotics, addressing the growing issue of antibiotic resistance.
Used in Antifungal Applications:
In the field of antifungal research, 5-(2-Propenylthio)-2,4(1H,3H)-pyrimidinedione is used as a potential antifungal agent. Its potential to inhibit fungal growth and reduce the severity of fungal infections makes it a valuable compound for further investigation and development.
Used in Chemical Research:
5-(2-Propenylthio)-2,4(1H,3H)-pyrimidinedione is used as a research compound in the field of organic chemistry. Its unique structure and potential reactivity make it an interesting subject for studies on the synthesis, properties, and applications of heterocyclic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 73236-43-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,2,3 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73236-43:
(7*7)+(6*3)+(5*2)+(4*3)+(3*6)+(2*4)+(1*3)=118
118 % 10 = 8
So 73236-43-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O2S/c1-2-3-12-5-4-8-7(11)9-6(5)10/h2,4H,1,3H2,(H2,8,9,10,11)
73236-43-8Relevant academic research and scientific papers
Dinan,Bardos
, p. 569 - 572 (1980)
A series of S-alkylated derivatives of 5-mercapto-2'-deoxyuridine have been prepared by alkylation of the preformed nucleoside. Two of these compounds, the S-propargyl and S-allyl derivatives, have shown significant antiviral activity against Herpes simplex type 1 in HeLa TK- cells but appear to be less effective in this assay system than some previously reported 5-substituted 2'-deoxyuridines.
