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Methyl piperidine-4-carboxylate is a reactant for C-2 arylation of piperidines through directed transition metal-catalyzed sp3 C-H activation. It is used as a reactant for synthesis of antitubercular agents, aminopyrazine inhibitors, orally available naphthyridine protein kinase D inhibitors and a scalable catalyst from asymmetric hydrogenation of sterically demanding aryl enamide.
Hana Prokopcova; Sheba D.Bergman; Karel Aelvoet; Veerle Smout; Wouter Herrebout; Benjamin Van der Veken; Lieven Meerpoel; Bert U.W.Maes. C-2 arylation of piperidines through directed transition-metal-catalyzed sp3 C-H activation. Chemistry: A European Journal. 2010, 16,(44), 13063-13067.
Ahmed Kamal; Rajesh V.C.R.N.C. Shetti; Shaik Azeeza; S.Kaleem Ahmed; P.Swapna; A.Malla Reddy; Inshad Ali Khan; Sandeep Sharma; Sheikh Tasduq Abdullah. Anti-tubercular agents. Part 5: Synthesis and biological evaluation of benzothiadiazine 1,1-dioxide based congeners. European Journal of Medicinal Chemistry. 2010, 45,(10), 4545-4553.
Hazard Statements: H227-H315-H319-H335
Combustible liquid. Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.
Precautionary Statements: P210u-P261-P280a-P305+P351+P338-P405-P501a
Keep away from heat/sparks/open flames/hot surfaces. - No smoking. Avoid breathing dust/fume/gas/mist/vapours/spray. Wear protective gloves and eye/face protection. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.