181114-74-9 Usage
Uses
Used in Pharmaceutical Synthesis:
1-Benzyl-3-methyl-pyrrolidin-3-carboxylic acid is used as a key intermediate in the synthesis of various bioactive compounds, contributing to the development of new drugs with improved therapeutic properties.
Used in Antimicrobial Applications:
1-BENZYL-3-METHYL-PYRROLIDINE-3-CARBOXYLIC ACID is studied for its antimicrobial properties, potentially serving as an active ingredient in the development of new antimicrobial agents to combat resistant bacterial strains.
Used in Antiviral Applications:
1-Benzyl-3-methyl-pyrrolidin-3-carboxylic acid has been investigated for its antiviral properties, offering potential in the creation of new antiviral drugs to treat viral infections.
Used in Organic Chemistry:
In the field of organic chemistry, 1-Benzyl-3-methyl-pyrrolidin-3-carboxylic acid is utilized as a chiral building block, enabling the synthesis of complex molecules with specific stereochemistry, which is crucial for the development of enantioselective reactions and the production of enantiomerically pure compounds.
Used in Research Chemicals:
1-BENZYL-3-METHYL-PYRROLIDINE-3-CARBOXYLIC ACID is also employed in the synthesis of research chemicals, facilitating the exploration of new chemical reactions and the discovery of novel bioactive molecules for various applications in the pharmaceutical and chemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 181114-74-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,1,1 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 181114-74:
(8*1)+(7*8)+(6*1)+(5*1)+(4*1)+(3*4)+(2*7)+(1*4)=109
109 % 10 = 9
So 181114-74-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H17NO2/c1-13(12(15)16)7-8-14(10-13)9-11-5-3-2-4-6-11/h2-6H,7-10H2,1H3,(H,15,16)
181114-74-9Relevant academic research and scientific papers
A stereoselective cyclization strategy for the preparation of γ-lactams and their use in the synthesis of α-Methyl-β-proline
Banerjee, Souvik,Smith, Justin,Smith, Jillian,Faulkner, Caleb,Masterson, Douglas S.
, p. 10925 - 10930 (2013/02/22)
A straightforward stereoselective and enantiodivergent cyclization strategy for the construction of γ-lactams is described. The cyclization strategy makes use of chiral malonic esters prepared from enantiomerically enriched monoesters of disubstituted malonic acid. The cyclization occurs with the selective displacement of a substituted benzyl alcohol as the leaving group. A Hammett study illustrates that the cyclization is under electronic control. The resulting γ-lactam can be readily converted into a novel proline analogue.
