7470-21-5 Usage
Uses
Used in Organic Synthesis:
1-(3-methoxyphenanthren-9-yl)ethanone is used as an intermediate in the synthesis of various organic compounds. Its unique structure allows for further functionalization and modification, making it a valuable building block in the creation of new molecules with specific properties and applications.
Used in Pharmaceutical Research:
1-(3-methoxyphenanthren-9-yl)ethanone is utilized as a starting material or a key component in the development of new pharmaceuticals. Its potential pharmacological properties make it a promising candidate for the treatment of various medical conditions. Researchers can explore its interactions with biological targets and evaluate its efficacy and safety in preclinical and clinical studies.
Used in Chemical Research:
In the field of chemical research, 1-(3-methoxyphenanthren-9-yl)ethanone serves as a model compound for studying the properties and reactivity of phenanthrene derivatives. This can lead to a better understanding of the structure-activity relationships and help in the design of more effective and targeted molecules for various applications.
Overall, 1-(3-methoxyphenanthren-9-yl)ethanone is a versatile and promising chemical compound with applications in organic synthesis, pharmaceutical research, and chemical research. Its specific uses and applications may vary depending on the intended research or industrial purposes, making it a valuable asset in the development of new technologies and treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 7470-21-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7470-21:
(6*7)+(5*4)+(4*7)+(3*0)+(2*2)+(1*1)=95
95 % 10 = 5
So 7470-21-5 is a valid CAS Registry Number.
7470-21-5Relevant academic research and scientific papers
Biphenyl Cyclobutenone Photoelectrocyclizations
Dai, Changhang,Rainier, Jon D.,Schwartz, Zach,Song, Changqing,Zhao, Xuchen
, p. 15164 - 15176 (2021/10/20)
In this work, we demonstrate that readily available conjugated bis-aryl cyclobutenones undergo photoelectrocyclization reactions to give the corresponding dihydrophenanthrene cyclobutanones when exposed to 350 nm light, TFA, and TMSCl. We have also found that cyclobutenone electrocyclizations and cycloreversions are in equilibrium.
A facile synthesis of 2h-chromenes and 9-functionalized phenanthrenes through reactions between α,β-unsaturated compounds and arynes
Zhang, Tiexin,Huang, Xian,Wu, Luling
experimental part, p. 3507 - 3519 (2012/07/30)
Facile syntheses of 2H-chromenes or 9-functionalized phenanthrenes under mild conditions in moderate to good yields have been developed. They each involve annulations of arynes with α,β-unsaturated compounds bearing different electron-withdrawing groups (EWGs). Depending on the natures of the different EWGs, the reactions proceed by different pathways: enals react with arynes through a tandem [2+2] cycloaddition/thermal electrocyclic ring-opening/6e-electrocyclization sequence to afford 2H-chromenes, whereas acyl-/ethoxycarbonyl-/cyano-substituted styrenes undergo Diels-Alder reactions with arynes followed by aromatization to afford 9-functionalized phenanthrenes. The scope, limitations, regioselectivities and mechanisms have been studied and are discussed in detail. Depending on the natures of different EWGs in α,β-unsaturated compounds, the reactions between arynes and α,β-unsaturated compounds proceed by different tandem pathways to afford either 2H-chromenes or 9-functionalized phenanthrenes in a selective manner, which is of potential pharmaceutical interest.
