89115-93-5 Usage
Uses
Used in Pharmaceutical Industry:
2-Piperidinecarboxylic acid, 2-methyl-, methyl ester is used as a key intermediate in the synthesis of pharmaceuticals for the treatment of various diseases and conditions. Its role as a precursor allows for the development of new drugs with potential therapeutic benefits.
Used in Chemical Industry:
In the chemical industry, 2-Piperidinecarboxylic acid, 2-methyl-, methyl ester is utilized in the creation of organic compounds, contributing to the advancement of chemical research and the production of specialty chemicals.
Used in Research and Development:
2-Piperidinecarboxylic acid, 2-methyl-, methyl ester is employed as a research tool in the development of new drugs and compounds. Its unique properties make it an essential component in exploring novel chemical pathways and potential applications in medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 89115-93-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,1,1 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 89115-93:
(7*8)+(6*9)+(5*1)+(4*1)+(3*5)+(2*9)+(1*3)=155
155 % 10 = 5
So 89115-93-5 is a valid CAS Registry Number.
89115-93-5Relevant academic research and scientific papers
Tricyclic dihydroimidazopyrimidinone derivative, and preparation method, pharmaceutical composition and application thereof
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Paragraph 0321-0324, (2021/05/12)
The invention provides a compound as shown in a general formula (I), cis-trans isomers, enantiomers, diastereoisomers, racemes, solvates, hydrates or pharmaceutically acceptable salts or prodrugs of the compound, a preparation method of the compound, a pharmaceutical composition containing the compound and an application of the compound as aLp-PLA2 inhibitor, wherein R1, R2, Rx, Ra, Q, U, X, Y, m, n and A are defined in the specification.
REACTION OF SCHIFF BASES ANIONS WITH α,ω-DIHALOALKENES : SYNTHETIC ROUTE TO CYCLIC α-AMINOACID DERIVATIVES.
Joucla, M.,Goumzili El, M.
, p. 1681 - 1684 (2007/10/02)
Imine anions of α-aminoesters, obtained from LDA/THF, undergo copper-catalyzed substitution reactions with α,ω-dihaloalkanes to lead to ω-haloalkylimines which are converted to cyclic α-aminoacid derivatives under anionic and thermal conditions.
