7433-53-6 Usage
Uses
Used in Organic Synthesis:
[(1R,2S)-2-phenylcyclopentyl]benzene is used as a key intermediate in the synthesis of various organic compounds due to its unique structure and reactivity. Its chiral nature allows for the development of novel asymmetric catalysis and enantioselective synthesis strategies, which are crucial in creating enantiomerically pure compounds with specific biological activities.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, [(1R,2S)-2-phenylcyclopentyl]benzene is utilized as a starting material or a structural motif for the design and development of new pharmaceuticals. Its potential pharmacological properties and the ability to modify its structure make it a valuable tool for creating novel drug candidates with improved efficacy and selectivity.
Used in Asymmetric Catalysis and Enantioselective Synthesis:
The stereochemistry and chiral nature of [(1R,2S)-2-phenylcyclopentyl]benzene make it an interesting target for studying asymmetric catalysis and enantioselective synthesis strategies. These studies are essential for the development of more efficient and environmentally friendly synthetic methods, as well as for the production of enantiomerically pure compounds with specific biological activities.
Used in Pharmaceutical Industry:
[(1R,2S)-2-phenylcyclopentyl]benzene is used as a building block for the development of new drugs in the pharmaceutical industry. Its unique structure and potential pharmacological properties allow researchers to explore its applications in various therapeutic areas, such as central nervous system disorders, cardiovascular diseases, and oncology.
Used in Chemical Research and Development:
In the chemical research and development sector, [(1R,2S)-2-phenylcyclopentyl]benzene serves as a valuable compound for studying the fundamental aspects of chemical reactions, such as reaction mechanisms, stereoselectivity, and catalyst design. This knowledge can be applied to develop new synthetic methods, improve existing processes, and create innovative materials with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 7433-53-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,3 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7433-53:
(6*7)+(5*4)+(4*3)+(3*3)+(2*5)+(1*3)=96
96 % 10 = 6
So 7433-53-6 is a valid CAS Registry Number.
7433-53-6Relevant academic research and scientific papers
Synthesis of Medium-Sized Carbocycles by Gallium-Catalyzed Tandem Carbonyl-Olefin Metathesis/Transfer Hydrogenation
Djurovic, Alexandre,Vayer, Marie,Li, Zhilong,Guillot, Regis,Baltaze, Jean-Pierre,Gandon, Vincent,Bour, Christophe
supporting information, p. 8132 - 8137 (2019/10/14)
The first examples of a catalytic tandem process involving a ring-closing carbonyl-olefin metathesis and a transfer hydrogenation are described. 1,4-Cyclohexadiene has been used as an H2 surrogate to reduce the cyclic alkenes formed after the m
Synthesis of new chiral bis(triarylphosphine) ligands based on asymmetric hydrogenation of 4,5-diaryl-2-oxocyclopentanecarb oxylates
Fukuda, Norio,Mashima, Kazushi,Matsumura, Yoh-Ichi,Takaya, Hidemasa
, p. 7185 - 7188 (2007/10/02)
New chiral bis(triarylphosphine) ligands, trans-bis(3-diphenylphosphinophenyl)cyclopentane and trans-bis(2-diphenylphosphinophenyl)cyclopentane, have been prepared in optically pure forms based on asymmetric hydrogenation of 4,5-diaryl-2-oxocyclopentaneca
Intramolecular Reactions of 1,5-Diaryl-1,5-pentadiyl Radicals
Peyman, Anuschirwan,Beckhaus, Hans-Dieter,Ruechardt, Christoph
, p. 1027 - 1032 (2007/10/02)
Photochemical decomposition of 2,6-diarylcyclohexanones 1a-d yields 1,2-diarylcyclopentanes 4 and 1,5-diaryl-1-pentenes 5 by intramolecular reaction of the intermediate 1,5-diaryl-1,5-pentadiyls 3.The two stereoisomers cis-4 and trans-4 are formed in equa
