54060-73-0 Usage
Uses
Used in Fluorescent Dyes:
9-(2-Hydroxyethyl)anthracene is used as a fluorescent dye due to its ability to emit light upon exposure to certain wavelengths, making it suitable for applications in analytical chemistry, bioimaging, and as markers in various research fields.
Used in Organic Light-Emitting Diodes (OLEDs):
In the electronics industry, 9-(2-Hydroxyethyl)anthracene is utilized as a component in organic light-emitting diodes for its light-emitting properties, contributing to the development of more efficient and versatile display and lighting technologies.
Used in Optoelectronic Devices:
9-(2-HYDROXYETHYL)ANTHRACENE's optical properties also make it a candidate for use in other optoelectronic devices, where its ability to interact with light can be harnessed for various applications, such as sensors and photovoltaic cells.
Used as a Photoinitiator in Photopolymerization Reactions:
9-(2-Hydroxyethyl)anthracene has been studied for its potential as a photoinitiator, a substance that absorbs light and triggers chemical reactions, specifically in photopolymerization. This application is particularly relevant in the field of materials science, where it can be used to initiate the curing of polymers upon exposure to light, enabling new methods of manufacturing and material processing.
Check Digit Verification of cas no
The CAS Registry Mumber 54060-73-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,0,6 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 54060-73:
(7*5)+(6*4)+(5*0)+(4*6)+(3*0)+(2*7)+(1*3)=100
100 % 10 = 0
So 54060-73-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H14O/c17-10-9-16-14-7-3-1-5-12(14)11-13-6-2-4-8-15(13)16/h1-8,11,17H,9-10H2
54060-73-0Relevant academic research and scientific papers
Thermally induced substrate release via intramolecular cyclizations of Amino esters and Amino carbonates
Knipp, Ralph J.,Estrada, Rosendo,Sethu, Palaniappan,Nantz, Michael H.
supporting information, p. 3422 - 3429 (2014/05/06)
The relative cleavage of an alcohol from a panel of amino esters and amino carbonates via intramolecular cyclization was examined as a mechanism for substrate release. Thermal stability at 37 °C was observed only for the seven-membered ring progenitors. Applicability of the approach was illustrated by δ-lactam formation within a poly(dimethylsiloxane) microchannel for release of a captured fluorescent probe.
The scope of catalytic asymmetric hydroboration/oxidation with rhodium complexes of 1,1'-(2-diarylphosphino-1-naphthyl)isoquinolines
Doucet, Henri,Fernandez, Elena,Layzell, Timothy P.,Brown, John M.
, p. 1320 - 1330 (2007/10/03)
Preformed cationic Rh complexes of the title ligands are effective for the asymmetric hydroboration/oxidation of vinylarenes at ambient temperature. These vinylarenes may carry E- or Z-β substituents but not a substituents. Enantiomer excesses of up to 97% can be obtained in the most favourable cases. The enantioselectivity is moderately sensitive to the structure of the ligand: the difurylphosphino ligand gave superior results for electron-poor styrenes and the diphenylphosphino ligand the best results for electron-rich reactants. Mechanistic aspects are discussed.
