60404-98-0 Usage
Uses
Used in Pharmaceutical Applications:
2,3-dimethoxy-5-methyl-5-(3-methylbut-2-en-1-yl)cyclohex-2-ene-1,4-dione is used as a pharmaceutical compound for its biological activity. The specific reasons for its use in this industry are not provided in the materials, but its potential applications could include targeting specific biological pathways or serving as a precursor in the synthesis of other bioactive molecules.
Used in Research Applications:
In the research industry, 2,3-dimethoxy-5-methyl-5-(3-methylbut-2-en-1-yl)cyclohex-2-ene-1,4-dione is used as a chemical probe to study its interactions with biological systems. Its unique structure and functional groups may provide insights into new mechanisms of action or reveal novel chemical properties that could be exploited in the development of new drugs or therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 60404-98-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,0 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 60404-98:
(7*6)+(6*0)+(5*4)+(4*0)+(3*4)+(2*9)+(1*8)=100
100 % 10 = 0
So 60404-98-0 is a valid CAS Registry Number.
60404-98-0Relevant academic research and scientific papers
Allylation of quinones bu allylic indium reagents
Araki, Shuki,Katsumura, Nobuhito,Butsugan, Yasuo
, p. 7 - 24 (2007/10/02)
Allylation of a variety of quinones by allylic indium sesquihalides was studied.Reactions of unsubstituted p-benzoquinone with allylindium, prenylindium, and geranylindium reagents gave, after oxidation with silver oxide, the corresponding allylated quinones in good yields.These reactions appear to proceed via 1,2-addition of the allylic indium reagents at the γ-carbon followed by sigmatropic rearrangement.Substituted quinones reacted with allylindium reagent giving excellent yields of allylquinols, whereas with prenylindium and geranylindium reagents, trisubstituted quinones gave diprenylcyclohexene-1,4-diones and 2,3-disubstituted quinones gave mixtures of prnylhydroquinones and diprenylcyclohexene-1,4-diones.In the prenylation of haloquinones, 1,2-addition, sigmatropic rearrangement, and elimination of indium(III) halide occurred in sequence yielding prenylquinones. 2-Hydroxy- and 2-methoxy-1,4-naphthoquinones gave α-addition products with prenylindium and cinnamylindium reagents.
