548461-24-1 Usage
Uses
Used in Organic Synthesis:
(+/-)-2-[(2-nitrophenyl)methyl]cyclopentanone is used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. The nitro group in the molecule allows for further functionalization and modification, making it a valuable building block for the development of new chemical entities.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (+/-)-2-[(2-nitrophenyl)methyl]cyclopentanone is used as a key component in the synthesis of complex molecules with potential therapeutic applications. Its cyclopentanone moiety provides a stable and versatile scaffold for the attachment of various functional groups, facilitating the design and synthesis of novel drug candidates.
Used in Research and Development:
(+/-)-2-[(2-nitrophenyl)methyl]cyclopentanone is also utilized in research and development settings to explore its potential pharmacological properties. Studies on (+/-)-2-[(2-nitrophenyl)methyl]cyclopentanone can provide insights into its biological activity, mechanism of action, and potential applications in the treatment of various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 548461-24-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,8,4,6 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 548461-24:
(8*5)+(7*4)+(6*8)+(5*4)+(4*6)+(3*1)+(2*2)+(1*4)=171
171 % 10 = 1
So 548461-24-1 is a valid CAS Registry Number.
548461-24-1Relevant academic research and scientific papers
Diastereoselective synthesis of linear-fused tricyclic nitrogen heterocycles by a tandem reduction-reductive amination reaction
Bunce, Richard A.,Herron, Derrick M.,Lewis, Jason R.,Kotturi, Sharadsrikar V.,Holt, Elizabeth M.
, p. 101 - 106 (2007/10/03)
A two-step diastereoselective synthesis of linear-fused tricyclic nitrogen heterocycles has been developed from cyclic β-ketoesters. The cyclization substrates are readily prepared by alkylation of the methyl 2-oxo-cycloalkanecarboxylates with 2-nitrobenz
