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9-Ethoxyanthracene is an organic compound with the chemical formula C16H14O. It is a derivative of anthracene, a tricyclic aromatic hydrocarbon, with an ethoxy group (C2H5O) attached to the 9th carbon atom. 9-Ethoxyanthracene is characterized by its yellow crystalline appearance and is soluble in organic solvents such as ethanol and ether. 9-Ethoxyanthracene is primarily used as a chemical intermediate in the synthesis of various dyes, pharmaceuticals, and other organic compounds. It is also employed as a fluorescent probe in analytical chemistry due to its strong fluorescence properties. However, it is important to note that 9-ethoxyanthracene has potential health risks and should be handled with caution, as it may cause irritation to the eyes, skin, and respiratory system.

6487-28-1

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6487-28-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6487-28-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,8 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6487-28:
(6*6)+(5*4)+(4*8)+(3*7)+(2*2)+(1*8)=121
121 % 10 = 1
So 6487-28-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H14O/c1-2-17-16-14-9-5-3-7-12(14)11-13-8-4-6-10-15(13)16/h3-11H,2H2,1H3

6487-28-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-ethoxyanthracene

1.2 Other means of identification

Product number -
Other names 9-ethylthioanthracene

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:6487-28-1 SDS

6487-28-1Relevant academic research and scientific papers

Synthesis of 9-anthryl ethers from trans-9,10-dihydro-9,10- dimethoxyanthracene by acid-catalyzed transetherification

Keun, Sam Jang,Hee, Young Shin,Dae, Yoon Chi

experimental part, p. 1703 - 1707 (2009/12/24)

During a study of electrophilic aromatic addition reactions (Ad EAr) to anthracene, anthryl ethers at the C9-position of anthracene were obtained as the major products when trans-9,10-dihydro-9,10- dimethoxyanthracene was reacted (10 minutes at

Application of Lanthanoids to Organic Chemistry. Direct Alkoxylation of Anthracene

Sugiyama, Takashi

, p. 1013 - 1016 (2007/10/02)

Direct alkoxylation of anthracene with some lower alcohols and ethylene glycol monoalkyl ethers, or monoacetate were carried out in the presence of cerium(IV)tetrakis(trifluoro acetate), and expected alkoxylated anthracene derivatives were obtained.

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