74962-96-2 Usage
Uses
Used in Organic Synthesis:
2,3-dimethylanthracene-1,4,5,8-tetrone is utilized as a reagent in organic synthesis, contributing to the formation of complex organic molecules. Its unique structure and reactivity make it a valuable component in the synthesis of various organic compounds.
Used as a Dye Intermediate:
In the dye industry, 2,3-dimethylanthracene-1,4,5,8-tetrone serves as a dye intermediate, playing a crucial role in the production of dyes with specific color properties. Its chemical structure allows for the creation of dyes with desired characteristics for various applications.
Used in Polymerization Reactions:
2,3-dimethylanthracene-1,4,5,8-tetrone is recognized for its potential use as a radical initiator in polymerization reactions. Its ability to initiate the formation of polymer chains is valuable in the production of various polymeric materials with specific properties.
Used in Photochemical Reactions:
As a photooxidizing agent, 2,3-dimethylanthracene-1,4,5,8-tetrone is employed in the study of photochemical reactions. Its involvement in these reactions aids in understanding the behavior of molecules under the influence of light, which is essential for the development of new photochemical processes and applications.
It is important to handle and store 2,3-dimethylanthracene-1,4,5,8-tetrone with care due to its hazardous nature, as it can cause skin and eye irritation upon contact. Proper safety measures should be taken to minimize risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 74962-96-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,9,6 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74962-96:
(7*7)+(6*4)+(5*9)+(4*6)+(3*2)+(2*9)+(1*6)=172
172 % 10 = 2
So 74962-96-2 is a valid CAS Registry Number.
74962-96-2Relevant academic research and scientific papers
Electronic structure and near-infrared spectra of diquinone anion radicals
Almlof,Feyereisen,Jozefiak,Miller
, p. 1206 - 1214 (2007/10/02)
The preparation of several substituted anthracene diquinones (1,4,5,8-anthracenetetrones), 1,4,6,11- naphthacenetetrone, and 5,7,12,14-pentacenetetrone is reported. These compounds, which have two quinones separated by one aromatic ring, were reduced elec
Capture du paradimethoxyorthoquinodimethane:syntheses de quinones et d'un intermediaire de la daunomycinone
Laduranty, Joelle,Lepage, Lucette,Lepage, Yves
, p. 1161 - 1167 (2007/10/02)
New para-dimethoxyl and para-diacetoxy derivatives in the naphthalene, anthracene, naphthacene, naphtho(2,3-c)thiophene and benzo-c-thiophene series are synthesized via the trapping of o-quinodimethanes by various dienophiles.Among these compounds, and in
