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Piperidine is widely used to convert ketones to enamines. [23] Enamines derived from piperidine are substrates in the Stork enamine alkylation reaction. [24] Upon treatment with calcium hypochlorite, piperidine converts to N-chloropiperidine, a chloramine with the formula C 5 H 10 NCl.
Glutarimide is the organic compound with the formula (CH 2) 3 (CO) 2 NH. It is a white solid. The compound forms upon dehydration of the amide of glutaric acid. [2] The drug lenalidomide contains the substructure glutarimide (blue) Glutarimide is sometimes called 2,6-piperidinedione.
The molecular formula C 5 H 11 N (molar mass: 85.15 g/mol, exact mass: 85.0891 u) may refer to: Piperidine (hexahydropyridine) Cyclopentylamine (cyclopentanamine) 1-Methylpyrrolidine; 2-Methylpyrrolidine
4-Amino-2,2,6,6-tetramethyl-4-piperidine is an organic compound with the formula H 2 NCH(CH 2 CMe 2) 2 NH (where Me = CH 3). Classified as a diamine , it is a colorless oily liquid. The compound is an intermediate in the preparation of Bobbitt's salt , an oxidant used in organic synthesis.
A Knoevenagel condensation is demonstrated in the reaction of 2-methoxybenzaldehyde 1 with the thiobarbituric acid 2 in ethanol using piperidine as a base. [7] The resulting enone 3 is a charge transfer complex molecule.
2,6-Dimethylpiperidines are chemical compounds with the formula C 5 H 8 (CH 3) 2 NH. Three stereoisomers exist: the achiral (R,S)-isomer and the chiral (R,R)/(S,S) enantiomeric pair. . Dimethylpiperidines are derivatives of the heterocycle piperidine, wherein two hydrogen atoms are replaced by methyl grou
N-Formylpiperidine is an organic compound with the formula C 6 H 11 NO. It is the amide of formic acid and piperidine. It can be used as a polar aprotic solvent, with better hydrocarbon solubility than other amide solvents such as dimethylformamide (DMF). [1] It has also been used to transfer the formyl group to a Grignard reagent: [2]
3,5-Dimethylpiperidines are chemical compounds with the formula C 5 H 8 (CH 3) 2 NH. Two diastereomers exist: the achiral R,S isomer and the chiral R,R/S,S enantiomeric pair. 3,5-Dimethylpiperidine is a precursor to tibric acid. The compound is typically prepared by hydrogenation of 3,5-dimethylpyridine.