330828-28-9 Usage
Uses
Used in Pharmaceutical Research:
5-Cyclohexyl-3-(p-tolyl)-1,2,4-oxadiazole is employed as a bioactive compound for its potential pharmacological properties, making it a candidate for the development of new drugs. Its unique structure and properties allow it to be studied for therapeutic applications in treating certain diseases.
Used in Organic Chemistry:
In the field of organic chemistry, 5-Cyclohexyl-3-(p-tolyl)-1,2,4-oxadiazole is used as a precursor in the synthesis of various organic compounds. Its ability to participate in chemical reactions facilitates the creation of a range of valuable chemical products, enhancing the scope of chemical synthesis and compound development.
Used in Drug Development:
5-Cyclohexyl-3-(p-tolyl)-1,2,4-oxadiazole is utilized in the development of new drugs, where its potential bioactivity and pharmacological properties are harnessed to address specific medical conditions. Its role in drug discovery and design contributes to the advancement of pharmaceutical therapies.
Used in Chemical Synthesis:
As a precursor in chemical synthesis, 5-Cyclohexyl-3-(p-tolyl)-1,2,4-oxadiazole is instrumental in the preparation of other valuable chemical compounds. Its structural attributes and reactivity make it a versatile component in the synthesis of a diverse array of organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 330828-28-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,0,8,2 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 330828-28:
(8*3)+(7*3)+(6*0)+(5*8)+(4*2)+(3*8)+(2*2)+(1*8)=129
129 % 10 = 9
So 330828-28-9 is a valid CAS Registry Number.
330828-28-9Relevant academic research and scientific papers
Nakka, Mangarao,Tadikonda, Ramu,Nakka, Srinivas,Vidavalur, Siddaiah
, p. 520 - 525 (2016)
A convenient and efficient protocol has been developed for the synthesis of 1,2,4-triazoles, N-fused 1,2,4-triazoles and 1,2,4-oxadiazoles using molybdenum hexacarbonyl where, for the first time, molybdenum hexacarbonyl acts as a convenient and reliable s
