1617-98-7 Usage
Explanation
The compound is composed of 11 carbon atoms, 11 hydrogen atoms, 3 nitrogen atoms, and 1 oxygen atom.
Explanation
It belongs to a class of organic compounds containing a five-membered heterocyclic ring with oxygen and nitrogen atoms.
Explanation
The specific compound has an ethyl group (-CH2CH3) and a phenyl group (C6H5) attached to the oxadiazole ring, which influences its chemical properties and reactivity.
Explanation
It is used as a building block for the synthesis of various biologically active molecules, which can be further developed into potential drugs or therapeutic agents.
Explanation
The compound's specific properties, such as solubility, stability, and reactivity, as well as its potential applications in medicine and industry, are still being researched and explored.
Explanation
Due to its unique structure and properties, the compound can be used to create new molecules with potential biological activities, which can be beneficial in the development of new drugs or therapies.
Explanation
The oxadiazole ring is a characteristic feature of this compound, which contributes to its chemical properties and reactivity in various chemical reactions.
Explanation
The presence of the ethyl and phenyl groups on the oxadiazole ring affects the compound's reactivity, making it suitable for use in the synthesis of various biologically active molecules.
Explanation
The compound's potential use in the development of new drugs and therapies is a primary focus of research, as it may lead to the discovery of novel treatments for various diseases and conditions.
Class
Oxadiazole derivative
Structure
Ethyl and phenyl groups attached to the oxadiazole ring
Application
Pharmaceutical research and development
Exploration
Specific properties and potential applications
Biological Activity
Potential use in the synthesis of biologically active molecules
Heterocyclic Ring
Five-membered ring with oxygen and nitrogen atoms
Chemical Reactivity
Influenced by the ethyl and phenyl groups
Research Focus
Development of new drugs and therapies
Check Digit Verification of cas no
The CAS Registry Mumber 1617-98-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,1 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1617-98:
(6*1)+(5*6)+(4*1)+(3*7)+(2*9)+(1*8)=87
87 % 10 = 7
So 1617-98-7 is a valid CAS Registry Number.
1617-98-7Relevant articles and documents
A KHSO4 mediated facile synthesis of 2-amino-1,3,4-oxadiazole derivatives
Gan, Zongjie,Han, Lei,Hu, Xiangnan,Long, Binyu,Tang, Qiang,Tian, Binghua,Wang, Chenyu,Wang, Zifan,Wu, Yue,Yu, Yu
, (2021/08/18)
A novel, efficient and mild KHSO4 mediated synthesis for 2-amino-1,3,4-oxadiazoles has been established via the cyclodesulfurization of benzoylhydrazine and isothiocyanate derivatives in one pot. The reactions proceeded smoothly at room tempera
Regioselective synthesis of 2-amino-substituted 1,3,4-oxadiazole and 1,3,4-thiadiazole derivatives via reagent-based cyclization of thiosemicarbazide intermediate
Yang, Seung-Ju,Lee, Seok-Hyeong,Kwak, Hyun-Jung,Gong, Young-Dae
, p. 438 - 444 (2013/04/10)
A regioselective, reagent-based method for the cyclization reaction of 2-amino-1,3,4-oxadiazole and 2-amino-1,3,4-thiadiazole core skeletons is described. The thiosemicarbazide intermediate 3 was reacted with EDC·HCl in DMSO or p-TsCl, triethylamine in N-
O -iodoxybenzoic acid mediated oxidative desulfurization initiated domino reactions for synthesis of azoles
Chaudhari, Pramod S.,Pathare, Sagar P.,Akamanchi, Krishnacharaya G.
experimental part, p. 3716 - 3723 (2012/06/16)
A systematic exploration of thiophilic ability of o-iodoxybenzoic acid (IBX) for oxidative desulfurization to trigger domino reactions leading to new methodologies for synthesis of different azoles is described. A variety of highly substituted oxadiazoles, thiadiazoles, triazoles, and tetrazoles have been successfully synthesized in good to excellent yields, starting from readily accessible thiosemicarbazides, bis-diarylthiourea, 1,3-disubtituted thiourea, and thioamides.
