913721-75-2 Usage
Uses
Used in Medicinal Chemistry:
Ethanone, 1-[2-(phenylmethoxy)[1,1'-biphenyl]-3-yl]is utilized as a key intermediate in the synthesis of various pharmaceutical compounds due to its unique structure and functional groups. Its ability to form stable covalent bonds with other molecules makes it a promising candidate for drug development.
Used in Pharmaceutical Research:
In the pharmaceutical industry, Ethanone, 1-[2-(phenylmethoxy)[1,1'-biphenyl]-3-yl]is employed as a research compound to explore its potential therapeutic properties. Its unique structure allows for the investigation of its interactions with biological targets, which could lead to the discovery of new drugs with improved efficacy and safety profiles.
Further studies are necessary to fully understand the biological activity and potential uses of Ethanone, 1-[2-(phenylmethoxy)[1,1'-biphenyl]-3-yl]-. As research progresses, it is expected that Ethanone, 1-[2-(phenylmethoxy)[1,1'-biphenyl]-3-yl]- will find more applications in various fields, particularly in the development of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 913721-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,7,2 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 913721-75:
(8*9)+(7*1)+(6*3)+(5*7)+(4*2)+(3*1)+(2*7)+(1*5)=162
162 % 10 = 2
So 913721-75-2 is a valid CAS Registry Number.
913721-75-2Relevant academic research and scientific papers
WB4101-related compounds: New, subtype-selective α1- adrenoreceptor antagonists (or inverse agonists?)
Pallavicini, Marco,Budriesi, Roberta,Fumagalli, Laura,Ioan, Pierfranco,Chiarini, Alberto,Bolchi, Cristiano,Ugenti, Maria Paola,Colleoni, Simona,Gobbi, Marco,Valoti, Ermanno
, p. 7140 - 7149 (2007/10/03)
Our previous structure-affinity relationship study had considered the enantiomers of the naphthodioxane, tetrahydronaphthodioxane, and 2-methoxy-1-naphthoxy analogues (compounds 1, 3, and 2, respectively) of 2-(2,6-dimethoxyphenoxyethylaminomethyl)-1,4-be
