4923-66-4 Usage
Uses
Used in Dye Manufacturing:
1,2,3,4-tetrahydroanthracene-9,10-dione is used as an intermediate in the manufacturing of dyes due to its chemical properties that contribute to the color and stability of the dyes produced.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 1,2,3,4-tetrahydroanthracene-9,10-dione is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be a building block for the development of new drugs with potential therapeutic benefits.
Used in Organic Compound Synthesis:
1,2,3,4-tetrahydroanthracene-9,10-dione is utilized as a starting material in the synthesis of other organic compounds, broadening its applications across different chemical and industrial processes.
Used in Antioxidant and Anti-Inflammatory Research:
1,2,3,4-tetrahydroanthracene-9,10-dione has been studied for its potential antioxidant and anti-inflammatory properties, indicating its possible use in the development of treatments for conditions related to oxidative stress and inflammation. Further research is needed to fully understand and harness these properties for medical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 4923-66-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,2 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4923-66:
(6*4)+(5*9)+(4*2)+(3*3)+(2*6)+(1*6)=104
104 % 10 = 4
So 4923-66-4 is a valid CAS Registry Number.
4923-66-4Relevant academic research and scientific papers
Colloid and nanodimensional catalysts in organic synthesis: VI.1 Hydrogenation and hydrogenolysis of carbonyl compounds
Mokhov,Popov,Nebykov
, p. 1656 - 1661 (2015/01/09)
Aldehydes and ketones are found to be hydrogenated to alcohols with hydrogen at atmospheric pressure under the catalysis with nickel nanoparticles. The reaction under study may be used as technologically available and cheap method for hydrogenation of carbonyl groups. It is found that in the case of aromatic ketones hydrogenolysis of C=O bond with partial hydrogenation of aromatic groups takes place.
COMPLETE REVERSAL OF REGIOCHEMISTRY IN CYCLIC ACYLPALLADATION. NOVEL SYNTHESIS OF QUINONES.
Negishi, Ei-ichi,Tour, James M.
, p. 4869 - 4872 (2007/10/02)
Treatment of o-iodoaryl alkenyl ketones with CO (600 psi) in CH3CN in the presence of 5 mol percent of Pd(dba)2 and 1 equiv of NEt3 can give bicyclic and polycyclic quinones in high yields via acylpalladation in an "endo" mode, which appears to be totally
