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54060-73-0

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54060-73-0 Usage

General Description

9-(2-Hydroxyethyl)anthracene is a chemical compound with the molecular formula C17H14O. It is a derivative of anthracene, which is a polycyclic aromatic hydrocarbon. The compound contains a hydroxyl group and an ethyl group attached to the anthracene structure. It is commonly used as a fluorescent dye and has been studied for its potential use in various applications such as organic light-emitting diodes (OLEDs) and other optoelectronic devices. It has also been investigated for its potential as a photoinitiator in photopolymerization reactions. Overall, 9-(2-Hydroxyethyl)anthracene has shown promise for its unique optical and electronic properties, making it a valuable compound for further research and development in the field of materials science and technology.

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

54060-73-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-(2-Hydroxyethyl)anthracene

1.2 Other means of identification

Product number -
Other names 2-(9-Anthryl)ethanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:54060-73-0 SDS

54060-73-0Relevant articles and documents

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.

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