91144-81-9 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 5 carbon (C), 4 hydrogen (H), 4 nitrogen (N), and 2 oxygen (O) atoms.
2. Heterocyclic compound
Explanation
A heterocyclic compound is a cyclic compound that contains atoms of at least two different elements, in this case, nitrogen and oxygen.
3. Nitrogen and oxygen atoms in the structure
Explanation
The compound's structure includes both nitrogen and oxygen atoms, which contribute to its unique properties and potential applications.
4. Potential applications in the pharmaceutical industry
Explanation
Due to its unique structure and properties, 1,3,4-oxadiazol-2-ol, 5-pyrazinylmay be used in the development of new drugs, making it a valuable compound for pharmaceutical research.
5. Development of biologically active molecules
Explanation
Researchers studying the design and synthesis of biologically active molecules may find 1,3,4-oxadiazol-2-ol, 5-pyrazinylof interest due to its unique structure and properties.
6. Uses in materials science and agriculture
Explanation
Beyond the pharmaceutical industry, 1,3,4-oxadiazol-2-ol, 5-pyrazinylmay also have potential applications in other fields such as materials science and agriculture, showcasing its versatility.
7. Versatile compound
Explanation
The compound's unique structure and properties make it suitable for various applications across different industries, highlighting its versatility.
Check Digit Verification of cas no
The CAS Registry Mumber 91144-81-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,1,4 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 91144-81:
(7*9)+(6*1)+(5*1)+(4*4)+(3*4)+(2*8)+(1*1)=119
119 % 10 = 9
So 91144-81-9 is a valid CAS Registry Number.
91144-81-9Relevant academic research and scientific papers
Propylene oxide assisted one-pot, tandem synthesis of substituted-1,3,4- oxadiazole-2(3H)-ones in water
Yan, Xu,Zhou, Shuo,Wang, Yuanqiang,Ge, Zemei,Cheng, Tieming,Li, Runtao
experimental part, p. 7978 - 7983 (2012/09/21)
It has been developed for the synthesis of substituted-1,3,4-oxadiazole- 2(3H)-one derivatives via a novel one-pot, tandem procedure assisted by propylene oxide. The 5-substitued-1,3,4-oxadiazole-2(3H)-ones and 3,5-disubstitued-1,3,4-oxadiazole-2(3H)-ones were, respectively, obtained from three-component reaction of acylhydrazines, carbon disulfide, and propylene oxide, and four-component reaction of acylhydarazines, carbon disulfide, propylene oxide, and organic halides. The reactions were carried out using water as solvent in the presence of potassium phosphate to afford the expected products in good to excellent yields.
Antimycobacterial activity of new 3,5-disubstituted 1,3,4-oxadiazol-2(3H)-one derivatives. Molecular modeling investigations
Zampieri, Daniele,Mamolo, Maria Grazia,Laurini, Erik,Fermeglia, Maurizio,Posocco, Paola,Pricl, Sabrina,Banfi, Elena,Scialino, Giuditta,Vio, Luciano
experimental part, p. 4693 - 4707 (2009/10/24)
3H-1,3,4-Oxadiazol-2-one derivatives were synthesized and tested for their in vitro antimycobacterial activity. Oxadiazolone derivatives showed an interesting antimycobacterial activity against the reference strain of Mycobacterium tuberculosis H37Rv. Molecular modeling investigations were performed and showed that the active compounds possess all necessary features to target the protein active site of the mycobacterial cytochrome P450-dependent sterol 14α-demethylase in the sterol biosynthesis pathway as the calculated free energy of binding were in agreement with the corresponding MIC values.
