93072-94-7 Usage
Uses
Used in Pharmaceutical Research and Development:
2-(5-PIPERIDIN-4-YL-1,2,4-OXADIAZOL-3-YL)PYRAZINE is used as a chemical entity in pharmaceutical research for its potential biological activities. Its heterocyclic structure, including the piperidine ring, may contribute to its interaction with biological targets, offering opportunities for the development of new therapeutic agents.
Used in Drug Design and Synthesis:
In the field of medicinal chemistry, 2-(5-PIPERIDIN-4-YL-1,2,4-OXADIAZOL-3-YL)PYRAZINE is used as a building block for the design and synthesis of novel drug candidates. Its unique structural features can be leveraged to create compounds with specific pharmacological properties, targeting a range of diseases and conditions.
Used in Biological Activity Studies:
2-(5-PIPERIDIN-4-YL-1,2,4-OXADIAZOL-3-YL)PYRAZINE is utilized in biological activity studies to evaluate its potential as a lead compound for drug discovery. Researchers investigate its interactions with various biological targets to understand its mechanism of action and therapeutic potential.
Note: Since the provided materials do not specify particular applications or industries for 2-(5-PIPERIDIN-4-YL-1,2,4-OXADIAZOL-3-YL)PYRAZINE, the uses listed are general and based on the compound's potential in pharmaceutical and medicinal chemistry contexts. Further research would be required to identify specific applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 93072-94-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,0,7 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 93072-94:
(7*9)+(6*3)+(5*0)+(4*7)+(3*2)+(2*9)+(1*4)=137
137 % 10 = 7
So 93072-94-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H13N5O/c1-3-12-4-2-8(1)11-15-10(16-17-11)9-7-13-5-6-14-9/h5-8,12H,1-4H2
93072-94-7Relevant academic research and scientific papers
Synthesis of Aryltriazolyl Derivatives
Krishnan, R.,Seshadri, S.
, p. 616 - 619 (2007/10/02)
p-Nitrophenylacetic acid (3) is converted into its malondialdehyde derivative (5) by the Vilsmeier-Haack reaction.The derivative (5) has been utilized to synthesize 1,4-disubstituted p-phenylene derivatives (12, 13, 16 and 19) which have been evaluated as
