58905-26-3 Usage
Description
Ethanone, 1-phenyl-2-(1H-1,2,4-triazol-1-yl)is a chemical compound with the molecular formula C10H8N4O. It belongs to the ketone and triazole families, featuring a phenyl group attached to a 1,2,4-triazole ring. Ethanone, 1-phenyl-2-(1H-1,2,4-triazol-1-yl)has a diverse range of applications and is valued for its potential in pharmaceuticals, agriculture, and research.
Uses
Used in Pharmaceutical Industry:
Ethanone, 1-phenyl-2-(1H-1,2,4-triazol-1-yl)is utilized as a building block in the synthesis of pharmaceutical compounds. Its unique structure allows it to be a key component in the development of new drugs, contributing to advancements in medicine.
Used in Agricultural Industry:
In agriculture, Ethanone, 1-phenyl-2-(1H-1,2,4-triazol-1-yl)may have potential applications as an antifungal, antiviral, or antiparasitic agent. Its biological activities can be harnessed to protect crops and enhance agricultural productivity.
Used in Research:
Ethanone, 1-phenyl-2-(1H-1,2,4-triazol-1-yl)also serves as a research tool in biochemical studies. Its properties and interactions with other compounds can provide valuable insights into various biological processes and contribute to the understanding of complex chemical reactions.
Overall, Ethanone, 1-phenyl-2-(1H-1,2,4-triazol-1-yl)is a versatile chemical compound with significant applications across different industries, making it an important substance for ongoing research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 58905-26-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,9,0 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58905-26:
(7*5)+(6*8)+(5*9)+(4*0)+(3*5)+(2*2)+(1*6)=153
153 % 10 = 3
So 58905-26-3 is a valid CAS Registry Number.
58905-26-3Relevant articles and documents
Asymmetric transfer hydrogenation of heterocycle-containing acetophenone derivatives using N-functionalised [(benzene)Ru(II)(TsDPEN)] complexes
Barrios-Rivera, Jonathan,Xu, Yingjian,Clarkson, Guy J.,Wills, Martin
supporting information, (2021/12/02)
The application of enantiomerically-pure ruthenium(II) catalysts containing N - functionalised TsDPEN ligand to the asymmetric transfer hydrogenation of 15 examples of α-heterocyclic acetophenone derivatives is reported. Products of up to 99% ee were formed.
Novel triazole-containing allyl benzoic acid ester compound as well as preparation method and application thereof
-
Paragraph 0028-0030, (2020/09/09)
The invention discloses a novel triazole-containing allyl benzoic acid ester compound as well as a preparation method and application thereof. The structural formula of the novel triazole-containing allyl benzoic acid ester compound is shown as a formula
Synthesis and Biological Evaluation of Novel Triazole Derivatives as Strigolactone Biosynthesis Inhibitors
Kawada, Kojiro,Takahashi, Ikuo,Arai, Minori,Sasaki, Yasuyuki,Asami, Tadao,Yajima, Shunsuke,Ito, Shinsaku
, p. 6143 - 6149 (2019/06/13)
Strigolactones (SLs) are one of the plant hormones that control several important agronomic traits, such as shoot branching, leaf senescence, and stress tolerance. Manipulation of the SL biosynthesis can increase the crop yield. We previously reported tha
