90923-05-0 Usage
Uses
Used in Organic Synthesis:
Ethanone, 1-(3,6-dimethoxy-2-nitrophenyl)is used as a key intermediate in the synthesis of various organic compounds, including pharmaceuticals and dyes. Its unique functional groups facilitate its incorporation into complex molecular structures, making it a valuable component in the development of new chemical entities.
Used in Biochemical Research:
In the field of biochemical research, Ethanone, 1-(3,6-dimethoxy-2-nitrophenyl)is utilized as a reagent to study the interactions and reactions of different biomolecules. Its presence can help researchers understand the mechanisms of various biological processes and potentially lead to the discovery of new therapeutic agents.
Used in Pharmaceutical Development:
Ethanone, 1-(3,6-dimethoxy-2-nitrophenyl)is used as a building block in the pharmaceutical industry for the synthesis of new drugs. Its versatile chemical structure allows for the creation of molecules with potential therapeutic applications, contributing to the advancement of medicine.
Used in Antimicrobial Applications:
Ethanone, 1-(3,6-dimethoxy-2-nitrophenyl)has been studied for its antimicrobial properties, making it a potential candidate for use in the development of new antimicrobial agents. Its ability to inhibit the growth of microorganisms could be harnessed in the formulation of new treatments for bacterial and fungal infections.
Used in Antioxidant Formulations:
Due to its antioxidant properties, Ethanone, 1-(3,6-dimethoxy-2-nitrophenyl)is considered for use in antioxidant formulations. It may be incorporated into products designed to protect cells from oxidative damage, potentially playing a role in the prevention of various diseases associated with oxidative stress.
Check Digit Verification of cas no
The CAS Registry Mumber 90923-05-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,9,2 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 90923-05:
(7*9)+(6*0)+(5*9)+(4*2)+(3*3)+(2*0)+(1*5)=130
130 % 10 = 0
So 90923-05-0 is a valid CAS Registry Number.
90923-05-0Relevant academic research and scientific papers
Studies on quinones: Part 30. Synthesis of benzo[b]thiophene-4,7- quinones
Valderrama, Jaime A.,Valderrama, Claudio
, p. 2143 - 2157 (2007/10/03)
The synthesis of a variety of benzo[b]thiophene-4,7-quinones (4a-f) by oxidative demethylation of the corresponding 4,7-dimethoxybenzo[b]thiophenes (3a-f) with cerium (IV) ammonium nitrate is reported. Heterocycles (3a,b) were prepared by cyclization of t
STUDIES ON THE SYNTHESIS OF FUSED HETEROCYCLES FROM o-AMINOCARBONYL COMPOUNDS
Fernandez, M.,Lopez, F.,Tapia, R.,Valderrama, J. A.
, p. 3087 - 3096 (2007/10/02)
Convenient preparations of 6-amino-2,5-dimethoxyacetophenone and benzaldehyde (3,6), and heterocyclization of these to produce benzisoxazol, quinoline amd cinnolinesystems are described.
Synthesis and Cardiotonic Activity of a Series of Substituted 4-Alkyl-2(1H)-quinazolinones
Bandurco, Victor T.,Schwender, Charles F.,Bell, Stanley C.,Combs, Donald W.,Kanojia, Ramesh M.,et al.
, p. 1421 - 1426 (2007/10/02)
The synthesis, cardiac fraction III cyclic nucleotide phosphodiesterase (PDE-III) inhibition, and positive inotropic activity of a series of 2(1H)-quinazolinones are reported.A general synthesis of the series involved the cyclization of 2-aminoacetophenones with potassium cyanate in acetic acid.Modifications at the 4-position of the quinazoline nucleus were best achieved by formation of the intermediate N1-acyl-N3-phenylurea from the substituted phenyl isocyanate and appropriate carboxamide.PPA was used to ring close to the quinazoline product.Generally the SAR for the series paralleled the five-point model previously published for PDE-III inhibition.The most active analogue of the series was 5,6-dimethoxy-4-methyl-2(1H)-quinazolinone (1) (ORF 16600), which had about twice the intravenous potency of amrinone.Compound 1 is currently under development as an orally active cardiotonic.
