69741-92-0 Usage
Uses
Used in Pharmaceutical Industry:
1,3,4-Oxadiazol-2-amine,5-(1,1-dimethylethyl)-(9CI) is used as a pharmaceutical intermediate for the development of new drugs. Its unique structure and properties make it a valuable compound for exploring its biological activities and pharmacological effects, which may contribute to the treatment of various diseases.
Used in Drug Discovery:
In the field of drug discovery, 1,3,4-Oxadiazol-2-amine,5-(1,1-dimethylethyl)-(9CI) serves as a key building block for the synthesis of novel compounds with potential therapeutic applications. Its presence in a molecule can influence the compound's pharmacokinetic and pharmacodynamic properties, making it an important component in the design of new drugs.
Used in Medicinal Chemistry Research:
1,3,4-Oxadiazol-2-amine,5-(1,1-dimethylethyl)-(9CI) is utilized in medicinal chemistry research to investigate its potential as a therapeutic agent. Studies on 1,3,4-Oxadiazol-2-amine,5-(1,1-dimethylethyl)-(9CI) may focus on understanding its mechanism of action, target engagement, and efficacy in treating specific diseases, ultimately contributing to the advancement of new treatment options.
Overall, 1,3,4-Oxadiazol-2-amine,5-(1,1-dimethylethyl)-(9CI) holds significant potential in the pharmaceutical industry, with its unique structure and properties making it a valuable asset for drug discovery, development, and research.
Check Digit Verification of cas no
The CAS Registry Mumber 69741-92-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,4 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69741-92:
(7*6)+(6*9)+(5*7)+(4*4)+(3*1)+(2*9)+(1*2)=170
170 % 10 = 0
So 69741-92-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H11N3O/c1-6(2,3)4-8-9-5(7)10-4/h1-3H3,(H2,7,9)
69741-92-0Relevant academic research and scientific papers
Synthesis of 2-amino-1,3,4-oxadiazoles and 2-Amino-1,3,4-thiadiazoles via sequential condensation and I2-mediated oxidative C-O/C-S bond formation
Niu, Pengfei,Kang, Jinfeng,Tian, Xianhai,Song, Lina,Liu, Hongxu,Wu, Jie,Yu, Wenquan,Chang, Junbiao
, p. 1018 - 1024 (2015/01/30)
2-Amino-substituted 1,3,4-oxadiazoles and 1,3,4-thiadiazoles were synthesized via condensation of semicarbazide/thiosemicarbazide and the corresponding aldehydes followed by I2-mediated oxidative C-O/C-S bond formation. This transition-metal-free sequential synthesis process is compatible with aromatic, aliphatic, and cinnamic aldehydes, providing facile access to a variety of diazole derivatives bearing a 2-amino substituent in an efficient and scalable fashion.
