306298-23-7 Usage
Uses
Used in Chemical Synthesis:
2-Methoxy-1-(4-(trifluoroMethyl)phenyl)ethanol is used as a solvent and reagent in chemical reactions for its ability to dissolve a wide range of substances and facilitate specific reaction pathways. Its unique structure allows it to participate in various organic synthesis processes, making it valuable in the production of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Solvent Applications:
As a solvent, 2-Methoxy-1-(4-(trifluoroMethyl)phenyl)ethanol is employed across different industries for its capacity to dissolve other compounds, which is essential in processes such as extraction, purification, and the formation of solutions for various chemical reactions.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-Methoxy-1-(4-(trifluoroMethyl)phenyl)ethanol is used as an intermediate in the synthesis of active pharmaceutical ingredients. Its unique properties enable the creation of new drug molecules with potential therapeutic benefits.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, 2-Methoxy-1-(4-(trifluoroMethyl)phenyl)ethanol serves as a key intermediate in the synthesis of various agrochemical products, contributing to the development of effective pesticides and other agricultural chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 306298-23-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,6,2,9 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 306298-23:
(8*3)+(7*0)+(6*6)+(5*2)+(4*9)+(3*8)+(2*2)+(1*3)=137
137 % 10 = 7
So 306298-23-7 is a valid CAS Registry Number.
InChI:InChI=1S/C10H11F3O2/c1-15-6-9(14)7-2-4-8(5-3-7)10(11,12)13/h2-5,9,14H,6H2,1H3
306298-23-7Relevant academic research and scientific papers
Tandem Acid/Pd-Catalyzed Reductive Rearrangement of Glycol Derivatives
Ciszek, Benjamin,Fleischer, Ivana,Kathe, Prasad,Schmidt, Tanno A.
supporting information, p. 3641 - 3646 (2020/03/25)
Herein, we describe the acid/Pd-tandem-catalyzed transformation of glycol derivatives into terminal formic esters. Mechanistic investigations show that the substrate undergoes rearrangement to an aldehyde under [1,2] hydrogen migration and cleavage of an oxygen-based leaving group. The leaving group is trapped as its formic ester, and the aldehyde is reduced and subsequently esterified to a formate. Whereas the rearrangement to the aldehyde is catalyzed by sulfonic acids, the reduction step requires a unique catalyst system comprising a PdII or Pd0 precursor in loadings as low as 0.75 mol % and α,α′-bis(di-tert-butylphosphino)-o-xylene as ligand. The reduction step makes use of formic acid as an easy-to-handle transfer reductant. The substrate scope of the transformation encompasses both aromatic and aliphatic substrates and a variety of leaving groups.
Piperazine derivatives useful as CCR5 antagonists
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Page column 115, (2010/02/05)
The use of CCR5 antagonists of the formula or a pharmaceutically acceptable salt thereof, wherein R is optionally substituted phenyl, pyridyl, thiophenyl or naphthyl; R1is hydrogen or alkyl; R2is substituted phenyl, substituted heter
