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Methyl piperidine-4-carboxylate, 98%, Thermo Scientific Chemicals
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化學識別
IUPAC Namemethyl piperidine-4-carboxylate
Molecular FormulaC7H13NO2
InChI KeyRZVWBASHHLFBJF-UHFFFAOYSA-N
SMILESCOC(=O)C1CCNCC1
Molecular Weight (g/mol)143.19
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規格
規格表
規格表Assay (GC)>97.5%
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.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
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.
Solubility
Slightly soluble in water.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
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.
Solubility
Slightly soluble in water.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- 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.