124190-19-8 Usage
Explanation
The compound consists of 18 carbon atoms, 18 hydrogen atoms, and 8 oxygen atoms.
Explanation
The total mass of one mole of the compound, calculated from the molecular formula.
Explanation
The compound's structure is characterized by these functional groups, which contribute to its chemical properties and potential applications.
Explanation
The core structure of the compound is based on the phenalene-1,3(2H)-dione backbone, which provides a foundation for the attachment of the functional groups.
Explanation
A propyl-oxo side chain is attached to the main structure, which may influence the compound's solubility, reactivity, and other properties.
Explanation
The compound may have potential uses in the pharmaceutical industry due to its structural features, such as antioxidant, anti-inflammatory, or antimicrobial properties.
Explanation
While the compound has potential applications, further research and testing are required to determine its specific properties and suitability for use in various industries.
Molecular weight
374.33 g/mol
Chemical structure
Three hydroxyl groups, a methoxy group, a methyl group, and two carbonyl groups
Derived from
Phenalene-1,3(2H)-dione backbone
Propyl-oxo side chain
2-(2-oxopropyl)
Potential applications
Pharmaceuticals
Further research needed
Specific properties and potential uses in medicine, agriculture, or materials science
Check Digit Verification of cas no
The CAS Registry Mumber 124190-19-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,1,9 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 124190-19:
(8*1)+(7*2)+(6*4)+(5*1)+(4*9)+(3*0)+(2*1)+(1*9)=98
98 % 10 = 8
So 124190-19-8 is a valid CAS Registry Number.
124190-19-8Relevant articles and documents
Total Syntheses of FR-901235, Auxarthrones A-D, and Lamellicolic Anhydride
Kiyotaki, Kotaro,Kayukawa, Takuto,Imayoshi, Ayumi,Tsubaki, Kazunori
, p. 9220 - 9224 (2020)
In our previous study, an unusual rearrangement reaction was discovered whereby dinaphthyl ketones with three hydroxy groups at restricted positions were transformed into a phenalenone ring and a benzene ring. Using the rearrangement as a key reaction, the first total syntheses of FR-901235 and auxarthrones A-D from an unstable triketone common intermediate are described. Furthermore, lamellicolic anhydride was synthesized from the triketone. This conversion is part of the putative biosynthetic pathway and was achieved experimentally for the first time.