110336-19-1 Usage
Uses
Used in Pharmaceutical Industry:
2,3-dihydro-1H-cyclopenta[c]phenanthren-1-one is used as a precursor in the synthesis of various pharmaceuticals for its ability to be chemically modified and incorporated into complex molecular structures, contributing to the development of new drugs and therapeutic agents.
Used in Organic Chemistry Research:
2,3-dihydro-1H-cyclopenta[c]phenanthren-1-one is used as a research chemical in the study of organic chemistry, allowing scientists to explore its reactivity, properties, and potential applications in the synthesis of novel compounds.
Used in Chemical Industry:
2,3-dihydro-1H-cyclopenta[c]phenanthren-1-one is used as a building block in the creation of synthetic compounds, enabling the development of new materials and products with specific properties and applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 110336-19-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,3,3 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 110336-19:
(8*1)+(7*1)+(6*0)+(5*3)+(4*3)+(3*6)+(2*1)+(1*9)=71
71 % 10 = 1
So 110336-19-1 is a valid CAS Registry Number.
110336-19-1Relevant academic research and scientific papers
Gacs-Baitz, Eszter,Minuti, Lucio,Taticchi, Aldo
, p. 10359 - 10366 (1994)
The Diels-Alder reactions of 4-acetoxy-2-cyclopenten-1-one and 2-bromo-4- acetoxy-2-cyclopenten-1-one with vinylarenes are discussed. The aromatization of the reaction products opens a new two-step route for the synthesis of cyclopentaphenanthrenones. Structure analysis of reaction products by 1H and 13C-NMR spectroscopy is reported.
Minuti, Lucio,Taticchi, Aldo,Gacs-Baitz, Eszter,Marrocchi, Assunta
, p. 8953 - 8958 (1995)
A new shorter synthesis of 2-vinyl-3,4-dihydro-naphthalene has been described.The Diels-Alder reactions of this diene with 4-acetoxy-2-cyclopenten-1-one, 3-bromoindan-1-one and inden-1-one under high pressure conditions are reported.A two step synthesis of cyclopenta- and indenophenanthrenones is discussed.Structure analysis by 1H and 13C NMR spectroscopy is presented.
