40538-50-9 Usage
Uses
Used in Pharmaceutical Synthesis:
1-methyl-1-(2-oxo-2-phenylethyl)piperidinium is used as a precursor in the synthesis of various pharmaceuticals and organic compounds. Its unique structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Organic Reactions:
1-methyl-1-(2-oxo-2-phenylethyl)piperidinium is employed as a catalyst in organic reactions, facilitating the conversion of reactants to products and improving the efficiency of chemical processes. Its catalytic properties make it a valuable tool in the synthesis of complex organic molecules.
Used in Material Science:
1-methyl-1-(2-oxo-2-phenylethyl)piperidinium serves as a building block in the development of new materials, with potential applications in areas such as polymer chemistry and materials engineering. Its structural characteristics enable the creation of novel materials with unique properties.
Used in Neuropharmacology Research:
1-methyl-1-(2-oxo-2-phenylethyl)piperidinium has been studied for its potential pharmacological properties, including its role as an inhibitor of enzymes and receptors in the nervous system. This research could lead to the discovery of new therapeutic agents for the treatment of neurological disorders.
Overall, 1-methyl-1-(2-oxo-2-phenylethyl)piperidinium has a wide range of applications in the fields of chemistry, pharmaceuticals, and material science, making it an important compound for ongoing research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 40538-50-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,5,3 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 40538-50:
(7*4)+(6*0)+(5*5)+(4*3)+(3*8)+(2*5)+(1*0)=99
99 % 10 = 9
So 40538-50-9 is a valid CAS Registry Number.
40538-50-9Relevant academic research and scientific papers
INTRAMOLECULAR CATALYSIS IN THE ENOLISATION OF AMINOKETONES
Cox, Brian G.,Maria Paolo De,Fini Adamo
, p. 1647 - 1652 (2007/10/02)
Measurements are reported on the rates of halogenation of the aminoketones PhCO(CH2)nNC5H10, with n = 1-3 , and N-methyl-4-piperidone (V), and their N-methyl derivatives.The reactions are zero order with respect to halogen concentration, with the rate-determining step being the formation of the enol or enolate ion.Large rate accelerations relative to acetophenone and cyclohexanone were observed, and these cannot be explained entirely in terms of inductive (through-bond) effects of =NH+, =NMe+, or =N groups.Other important factors are (i) intramolecular stabilization of the developing negative charge by the positive ammonium ion, the maximum effects being observed for (II); (ii) electrostatic interactions with negatively charged catalysts; (iii) direct proton transfer from the ionising C-H group to =N, acting as an intramolecular base catalyst.Evidence for a direct proton transfer was found only in reactions of the γ-substituted aminoketone (IV).
