| Weight | 143.186 g/mol |
|---|---|
| Formula | C7H13NO2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
methyl piperidine-3-carboxylate (50585-89-2)
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- Blockade of 2-Arachidonoylglycerol Hydrolysis by Selective Monoacylglycerol Lipase Inhibitor 4-Nitrophenyl 4-(Dibenzo[d][1,3]dioxol-5-yl(hydroxy)methyl)piperidine-1-carboxylate (JZL184) Enhances Retrograde Endocannabinoid Signaling (Journal of Pharmacology and Experimental Therapeutics, 2009)
- Stereospecific route for the synthesis of 1,5-lactams : Synthesis of (2S,3S,4R,5R)-methyl-3,4,5-triphenylmethylenoxy-6-oxo-piperidine-2-carboxylate (Tetrahedron Letters, 1994)
- Synthesis of ethyl-4(3'-methoxyphenyl)-1-methyl piperidine-3-carboxylate (1981)
- Catalysis in aromatic nucleophilic substitution. Part 5. Reactions of piperidine with methyl 2-methoxy-3-nitrothiophen-5-carboxylate and 5-acetyl-2-methoxy-3-nitrothiophen (Journal of The Chemical Society-perkin Transactions 1, 1981)
- ChemInform Abstract: CATALYSIS IN AROMATIC NUCLEOPHILIC SUBSTITUTION. PART 5. REACTIONS OF PIPERIDINE WITH METHYL 2METHOXY3NITROTHIOPHENE5CARBOXYLATE AND 5ACETYL2METHOXY3NITROTHIOPHENE (ChemInform, 1981)
- ChemInform Abstract: Stereospecific Route for the Synthesis of 1,5-Lactams: Synthesis of ( 2S,3S,4R,5R)-Methyl-3,4,5-triphenylmethylenoxy-6-oxo-piperidine-2- carboxylate. (ChemInform, 2010)
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SMILESCOC(=O)C1CCCNC1
-
InChIKeyBCDBHIAXYFPJCT-UHFFFAOYSA-N
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