299936-83-7 Usage
Uses
Used in Pharmaceutical Industry:
5-(2-ETHOXY-ETHYL)-[1,3,4]THIADIAZOL-2-YLAMINE is used as a potential active pharmaceutical ingredient for its possible anticancer properties. 5-(2-ETHOXY-ETHYL)-[1,3,4]THIADIAZOL-2-YLAMINE's thiadiazole ring is known to exhibit such activity, and the presence of the amine group may enhance its interaction with biological targets, making it a candidate for further development in cancer treatment.
Used in Antiviral Applications:
In the field of antiviral research, 5-(2-ETHOXY-ETHYL)-[1,3,4]THIADIAZOL-2-YLAMINE may be utilized as a starting point for the development of new antiviral drugs. 5-(2-ETHOXY-ETHYL)-[1,3,4]THIADIAZOL-2-YLAMINE's structure could allow it to interfere with viral replication or entry into host cells, thus providing a therapeutic advantage against viral infections.
Used in Antimicrobial Applications:
5-(2-ETHOXY-ETHYL)-[1,3,4]THIADIAZOL-2-YLAMINE is also considered for use in antimicrobial applications, given the known antimicrobial properties of thiadiazole compounds. 5-(2-ETHOXY-ETHYL)-[1,3,4]THIADIAZOL-2-YLAMINE could be further optimized to target specific pathogens, contributing to the development of new antibiotics or antifungal agents.
Used in Drug Delivery Systems:
5-(2-ETHOXY-ETHYL)-[1,3,4]THIADIAZOL-2-YLAMINE's ethoxyethyl group may be leveraged in the design of drug delivery systems, potentially improving the solubility and bioavailability of 5-(2-ETHOXY-ETHYL)-[1,3,4]THIADIAZOL-2-YLAMINE. This could be particularly useful in the development of formulations that enhance the compound's therapeutic efficacy and reduce side effects.
Used in Medicinal Chemistry Research:
5-(2-ETHOXY-ETHYL)-[1,3,4]THIADIAZOL-2-YLAMINE serves as a valuable compound in medicinal chemistry research, where it can be studied for its potential to interact with various biological targets. Understanding its binding properties and mechanisms of action can lead to the discovery of new drugs with improved pharmacological profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 299936-83-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,9,9,3 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 299936-83:
(8*2)+(7*9)+(6*9)+(5*9)+(4*3)+(3*6)+(2*8)+(1*3)=227
227 % 10 = 7
So 299936-83-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H11N3OS/c1-2-10-4-3-5-8-9-6(7)11-5/h2-4H2,1H3,(H2,7,9)
299936-83-7Relevant academic research and scientific papers
Kukaniev,Osimov,Sangov,Safarov,Karimov,Radjabov
, p. 882 - 885 (2008)
A one-pot method has been developed for the synthesis of 2-R-7-methyl-5-oxo-5H-1,3,4-thia-diazolo[3,2-a]pyrimidine by condensation of β-alkylthio(alkoxy)propionitrile, thiosemicarbazide, and ethyl acetoacetate in PPA, and also (7-methyl-5-oxo-5H-1,3,4-thidiazolo[3,2-a]pyrimidin-2-yl)- acetamide from cyanoacetamide, thiosemicarbazide, and ethyl acetoacetate.
