91910-07-5 Usage
Appearance
Yellow crystalline solid
The compound appears as a yellow solid with a crystalline structure.
Structure
Naphthoquinone backbone with a methoxy group attached
The compound has a naphthoquinone core structure, which is a fused bicyclic ring system consisting of a benzene ring and a six-membered ring with one oxygen atom. A methoxy group (-OCH3) is attached to this backbone.
Biological activities
Anti-cancer, anti-inflammatory, and anti-microbial properties
1-methoxy-1,4,4a,8a-tetrahydro-1,4-ethanonaphthalene-5,8-dione has been found to exhibit various biological activities, such as inhibiting the growth of cancer cells, reducing inflammation, and fighting against microorganisms.
Therapeutic potential
Potential use as a therapeutic agent for various health conditions
Due to its biological activities, the compound has been studied for its potential as a treatment for a range of health conditions, including cancer, inflammation, and infections.
Synthesis
Utilized as a starting material in the synthesis of other organic compounds
1-methoxy-1,4,4a,8a-tetrahydro-1,4-ethanonaphthalene-5,8-dione can also be used as a precursor in the synthesis of other organic compounds, making it a valuable building block in organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 91910-07-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,9,1 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 91910-07:
(7*9)+(6*1)+(5*9)+(4*1)+(3*0)+(2*0)+(1*7)=125
125 % 10 = 5
So 91910-07-5 is a valid CAS Registry Number.
91910-07-5Relevant articles and documents
Synthesis of 1,5-dimethoxy-4-naphthol and 2-allyl-5-methoxy-1,4-naphthoquinone. A new approach
Hugo,Snijman,Green
, p. 577 - 584 (1993)
Convenient syntheses for 1,5-dimethoxy-4-naphthol and 2-allyl-5-methoxy-1,4-naphthoquinone have been developed. A key step in the formation of the title compounds involved methylation or allylation of an intermediate Diels-Alder adduct.
Synthesis of 3-acetyl-5-methoxy-1,4-naphthoquinone. A new approach
Hugo,Nicholson,Snijman
, p. 23 - 28 (1994)
A new and efficient synthesis for 3-acetyl-5-methoxy-1,4- naphthoquinone has been developed. The synthesis involves inter alia pyrolysis of an acetylated Diels-Alder adduct and a regiospecific Fries rearrangement reaction.
