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  2. 4-Piperidone - Wikipedia

    en.wikipedia.org/wiki/4-Piperidone

    4-Piperidone is an organic compound with the molecular formula OC(CH 2) 4 NH. It can be viewed as a derivative of piperidine. 4-Piperidone is used as an intermediate in the manufacture of chemicals and pharmaceutical drugs. Substituted and dehydro derivatives of 4-piperidinone are intermediates in alkaloid syntheses. [1]

  3. Piperylone - Wikipedia

    en.wikipedia.org/wiki/Piperylone

    Hydrazone formation of 1-methyl-4-piperidone (1) with benzohydrazide (2) gives (3). Catalytic hydrogenation using Adams' catalyst gives the substituted hydrazine (6) after acid-catalyzed hydrolysis to remove the benzoyl group and neutralization.

  4. Piperidine - Wikipedia

    en.wikipedia.org/wiki/Piperidine

    N-Methyl-3-piperidyl benzilate (JB-336, BZ) Piperidine is also commonly used in chemical degradation reactions, such as the sequencing of DNA in the cleavage of particular modified nucleotides . Piperidine is also commonly used as a base for the deprotection of Fmoc - amino acids used in solid-phase peptide synthesis .

  5. Pempidine - Wikipedia

    en.wikipedia.org/wiki/Pempidine

    Pempidine is an aliphatic, sterically hindered, cyclic, tertiary amine, which is a weak base: in its protonated form it has a pK a of 11.25. [4]Pempidine is a liquid with a boiling point of 187–188 °C and a density of 0.858 g/cm 3.

  6. 4-Pyridone - Wikipedia

    en.wikipedia.org/wiki/4-Pyridone

    4-Pyridone is an organic compound with the formula C 5 H 4 NH(O). It is a colorless solid. Preparation. ... 4-Piperidone; Dehydroacetic acid; References

  7. 2,2,6,6-Tetramethylpiperidine - Wikipedia

    en.wikipedia.org/wiki/2,2,6,6-tetramethylpiperidine

    2,2,6,6-Tetramethylpiperidine, abbreviated TMP, HTMP, or TMPH, is an organic compound of the amine class. In appearance, it is a colorless liquid and has a "fishy", amine-like odor.

  8. Piperidinone - Wikipedia

    en.wikipedia.org/wiki/Piperidinone

    Piperidinones or piperidones are a class of chemical compounds sharing the piperidone skeleton. A classic named reaction for the synthesis of piperidones is the Petrenko-Kritschenko piperidone synthesis which involves combining an alkyl-1,3-acetonedicarboxylate with benzaldehyde and an amine. [1]

  9. Piperidione - Wikipedia

    en.wikipedia.org/wiki/Piperidione

    Piperidione (trade name Sedulon) is a sedative drug, structurally related to methyprylon and pyrithyldione.It used to be marketed by Roche as a cough medicine available in liquid form.