63378-71-2 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
Ethyl 2-Oxo-3-Phenylpiperidine-3-Carboxylate is used as a research compound for the development of new pharmaceuticals. Its potential pharmacological activities, such as analgesic and anti-inflammatory properties, make it a valuable candidate for the creation of novel therapeutic agents.
Used in Pain Management:
Ethyl 2-Oxo-3-Phenylpiperidine-3-Carboxylate is used as an analgesic agent for the management of pain. Its ability to alleviate pain makes it a potential candidate for the development of pain relief medications.
Used in Anti-Inflammatory Treatments:
Ethyl 2-Oxo-3-Phenylpiperidine-3-Carboxylate is used as an anti-inflammatory agent to reduce inflammation and associated symptoms. Its potential to combat inflammation positions it as a candidate for the development of anti-inflammatory drugs.
Used in Neurodegenerative Disorder Treatment:
Ethyl 2-Oxo-3-Phenylpiperidine-3-Carboxylate is used as a potential therapeutic agent for the treatment of neurodegenerative disorders. Its study for this purpose indicates that it may have neuroprotective properties that could be harnessed in the development of treatments for conditions such as Alzheimer's disease or Parkinson's disease.
Used in Psychiatric Condition Management:
Ethyl 2-Oxo-3-Phenylpiperidine-3-Carboxylate is used as a potential agent for the management of psychiatric conditions. Its exploration in this area suggests that it may have applications in the development of medications for mental health disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 63378-71-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,3,7 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 63378-71:
(7*6)+(6*3)+(5*3)+(4*7)+(3*8)+(2*7)+(1*1)=142
142 % 10 = 2
So 63378-71-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H17NO3/c1-2-18-13(17)14(9-6-10-15-12(14)16)11-7-4-3-5-8-11/h3-5,7-8H,2,6,9-10H2,1H3,(H,15,16)
63378-71-2Relevant academic research and scientific papers
Influence of ring size on the outcome of sulfide contraction reactions with thiolactams. Isolation of bicyclic ketene S,N-acetals and thioisomuenchnones
Michael, Joseph P.,De Koning, Charles B.,Van der Westhuyzen, Christiaan W.,Fernandes, Manuel A.
, p. 2055 - 2062 (2007/10/03)
Reaction between diethyl bromomalonate and 3-phenylpyrrolidine-2-thione yielded a vinylogous urethane by the Eschenmoser sulfide contraction. However, with 3-substituted piperidine-2-thiones, sulfur was retained in the products, and a range of bicyclic heterocycles, including bicyclic ketene S,N-acetals (2-alkylidene-1,3-thiazolidin-4-ones) and stable thioisomuechnones, was isolated. A novel dimeric ketene S,N-acetal was characterised by X-ray crystallography.
Potential GABAB Receptor Antagonists. X* the Synthesis of Further Analogues of Baclofen, Phaclbfen and Saclofen
Prager, Rolf H.,Schafer, Karl
, p. 813 - 823 (2007/10/03)
In an attempt to obtain new compounds with binding activity at the GABAB receptor site, we report the synthesis of 3-amino-2-arylpropanoic acids, and the sulfonic, phosphonic and hydroxamic acid analogues. In addition, we report the synthesis of the isomer of phaclofen, 3-amino-1-(4-chlorophenyl)-propylphosphonic acid, and the higher homologue of baclofen, 5-amino-2-(4-chlorophenyl)pentanoic acid.
Synthesis of new deazatetrahydropterins as potential NO synthase modulators
Nallet, Jean-Pierre,Megard, Anne-Lise,Dreux, Jacques
, p. 491 - 500 (2007/10/03)
As part of our research on NO synthase modulators, a series of deazatetrahydropterins were synthesized and their effects were assessed. In this paper, we describe the synthesis of new substituted (especially at the 4a position) 2-amino-4-hydroxy-3,4,4a,5,6,7-hexahydropyrido[2,3-d]pyrimidines. These compounds showed no interesting pharmacological activity. Elsevier.
