107941-41-3 Usage
Chemical structure
A naphthalene derivative with a benzyl ether group, a methoxy group, and a propynyl group.
Appearance
It is likely a solid or oily liquid, although the exact appearance is not provided in the material.
Organic synthesis
Used as a building block for the preparation of various biologically active molecules and pharmaceuticals.
Medicinal chemistry
Has potential applications due to its ability to interact with biological targets such as enzymes and receptors.
Anti-inflammatory
Has been studied for its potential anti-inflammatory properties.
Anti-cancer
Has been studied for its potential anti-cancer properties.
Further research and development
It is an interesting compound for further research and development in the fields of medicinal chemistry and drug discovery.
Please note that some properties, such as appearance and solubility, are not provided in the material and may require additional research or experimentation to determine.
Check Digit Verification of cas no
The CAS Registry Mumber 107941-41-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,9,4 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 107941-41:
(8*1)+(7*0)+(6*7)+(5*9)+(4*4)+(3*1)+(2*4)+(1*1)=123
123 % 10 = 3
So 107941-41-3 is a valid CAS Registry Number.
107941-41-3Relevant academic research and scientific papers
Synthetic Approach to Aklavinone Using 2-Oxo-2H-pyran-5-carboxylate (Coumalate) Intermediates
Jung, Michael E.,Hagenah, Jeffrey A.
, p. 1889 - 1902 (2007/10/02)
A novel approach for the preparation of aklavinone 5 is described in which the key step is the cycloaddition of a substituted coumalate with a ketene acetal to produce a masked A ring with the C and D rings attached.The 4-(arylmethyl)coumalate 53 was prepared from naphthalene-1,5-diol (6) by a seven step route involving as the key step the cyclocondensation of the methyl (arylmethyl)propiolate 52 with methyl 3-oxopentanoate 10.Cycloaddition of 53 with dimethyl ketene acetal 12 produced the potential A-ring precursor 67, which could not be cleanly reduced, thereby ending this scheme.The preparation of functionalized 4,6-dialkylpyrone-5-carboxylates and their use in the synthesis of bicyclic lactones and substituted benzoates via cycloaddition reactions are also described.
