761360-22-9 Usage
Uses
Used in Pharmaceutical Industry:
2-Piperidinecarboxylic acid, 4-oxo-, methyl ester, (S)-(9CI) is used as a building block for the synthesis of various pharmaceuticals and biologically active compounds. Its unique chemical structure allows it to be incorporated into the development of new drugs and therapeutic agents.
Used in Research and Development:
In the field of research and development, 2-Piperidinecarboxylic acid, 4-oxo-, methyl ester, (S)-(9CI) serves as a valuable intermediate for the synthesis of complex organic molecules and the exploration of novel chemical reactions. Its versatility in chemical transformations makes it an essential tool for advancing scientific knowledge and discovering new applications.
Used in Chemical Synthesis:
2-Piperidinecarboxylic acid, 4-oxo-, methyl ester, (S)-(9CI) is utilized in chemical synthesis processes to create a wide range of compounds with diverse applications. Its reactivity and functional groups enable the formation of various chemical bonds, contributing to the development of new materials and products across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 761360-22-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,1,3,6 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 761360-22:
(8*7)+(7*6)+(6*1)+(5*3)+(4*6)+(3*0)+(2*2)+(1*2)=149
149 % 10 = 9
So 761360-22-9 is a valid CAS Registry Number.
761360-22-9Relevant academic research and scientific papers
PHENOXYETHYL CYCLIC AMINE DERIVATIVES AND THEIR ACTIVITY AS EP4 RECEPTOR MODULATORS
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Page/Page column 16; 17, (2015/07/07)
The present invention provides a compound of the Formula (I): wherein X, R, R1,R2,R3, R4,R5,R6, R7, R8, and R9 are as defined herein, or a pharmaceutically acceptable salt thereof.
AMINO ACID DERIVATIVES
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Page column 44, (2010/01/30)
There is provided amino acid derivatives of formula I, wherein p, q, R 1, R 2, R 3, R 4, Y, n and B have meanings given in the description which are useful as competitive inhibitors of trypsin-like proteases, such as thrombin, and in particular in the treatment of conditions where inhibition of thrombin is required (e.g. thrombosis) or as anticoagulants.
A new synthesis of (2S)-4-oxopipecolic acid by thermal rearrangement of enantiopure spirocyclopropaneisoxazolidine
Machetti, Fabrizio,Cordero, Franca M.,De Sarlo, Francesco,Guarna, Antonio,Brandi, Alberto
, p. 4205 - 4208 (2007/10/03)
A novel synthesis of (2S)-4-oxo-pipecolic acid is reported. The synthetic route employs as a key step the diastereoselective cycloaddition of the N- glycosylnitrone 7 to methylenecyclopropane followed by thermal rearrangement of the spirocyclopropaneisoxazolidine 8a. Stereoselective reduction of the N- BOC methyl ester of 4-oxopipecolic acid by L-selectride gives the protected cis-4-hydroxy-pipecolic acid 14.
