116140-49-9 Usage
Uses
Used in Pharmaceutical Industry:
3-Methylpiperidine-3-carboxylic acid is used as a key intermediate in the synthesis of various pharmaceutical drugs for its ability to contribute to the development of new medications with improved therapeutic profiles.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3-Methylpiperidine-3-carboxylic acid is utilized as a structural component in the design and synthesis of bioactive compounds, which can be further optimized for specific medical conditions.
Used in Drug Discovery:
3-Methylpiperidine-3-carboxylic acid is employed as a valuable intermediate in drug discovery processes, where its unique properties can be leveraged to create novel drug candidates with potential applications in treating a range of medical conditions.
Used in Organic Synthesis:
3-Methylpiperidine-3-carboxylic acid is also used as a versatile building block in organic synthesis, allowing for the creation of a variety of chemical entities that can be explored for their potential uses in different industries, including but not limited to pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 116140-49-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,1,4 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 116140-49:
(8*1)+(7*1)+(6*6)+(5*1)+(4*4)+(3*0)+(2*4)+(1*9)=89
89 % 10 = 9
So 116140-49-9 is a valid CAS Registry Number.
116140-49-9Relevant academic research and scientific papers
Banerjee, Souvik,Vogel, Emily R.,Hinton, Daniel,Sterling, Michael,Masterson, Douglas S.
, p. 1292 - 1299 (2015)
A stereoselective and enantiodivergent strategy for the construction of δ-lactams is described. The strategy utilizes chiral malonic esters prepared from enantiomerically enriched mono esters of disubstituted malonic acid. A cyclization occurs with the selective displacement of a substituted benzyl alcohol as the leaving group. The resulting δ-lactams are then converted into nipecotic acid analogues using straightforward transformations. The resulting nipecotic acid analogues proved capable organocatalysts in Mannich reactions.
