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604-66-0

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604-66-0 Usage

General Description

Diacetic acid 9,10-anthracenediyl ester is a chemical compound with the formula C24H16O4. It is a derivative of anthracene, which is a polycyclic aromatic hydrocarbon. Diacetic acid 9,10-anthracenediyl ester can be used in various applications, including as a fluorescent dye for biological and chemical research, as well as in organic synthesis as a building block for the preparation of other compounds. It is important to handle this chemical with care, as it may be harmful if ingested or inhaled, and can cause irritation to the skin and eyes. Proper safety precautions and handling procedures should be followed when working with diacetic acid 9,10-anthracenediyl ester.

Check Digit Verification of cas no

The CAS Registry Mumber 604-66-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 604-66:
(5*6)+(4*0)+(3*4)+(2*6)+(1*6)=60
60 % 10 = 0
So 604-66-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H14O4/c1-11(19)21-17-13-7-3-5-9-15(13)18(22-12(2)20)16-10-6-4-8-14(16)17/h3-10H,1-2H3

604-66-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name anthracene-9,10-diol diacetate

1.2 Other means of identification

Product number -
Other names 9,10-Anthracenediol,diacetate

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:604-66-0 SDS

604-66-0Relevant articles and documents

Intermediates in the cleavage of endoperoxides

Bauch, Marcel,Klaper, Matthias,Linker, Torsten

supporting information, (2017/03/24)

The decomposition of anthracene endoperoxides has been investigated under various conditions. Thermolyses proceed via radical intermediates and afford anthracenes and rearrangement products, depending on the substitution pattern. Interestingly, not only the O–O but also the C–O bond can be cleaved homolytically. Under basic conditions fragmentations take place, affording anthraquinone, and reactive oxygen species. This mechanism explains the often observed decomposition of endoperoxides during work-up. Finally, an acid-catalyzed cleavage has been observed under release of hydrogen peroxide. The results should be interesting for the mechanistic understanding of peroxide decomposition and the endoperoxides might serve as mild sources of reactive oxygen species for future applications. Copyright

Diene-Substituent Effects on the Rate of the Retro-Diels-Alder Reaction. Cycloreversion Reactivity Varying over a Range of Five Powers of Ten

Chung, Y.-S.,Duerr, Brook F.,Nanjappan, P.,Czarnik, Anthony W.

, p. 1334 - 1336 (2007/10/02)

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