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  2. Piperidine - Wikipedia

    en.wikipedia.org/wiki/Piperidine

    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.

  3. Piperine - Wikipedia

    en.wikipedia.org/wiki/Piperine

    Due to its poor solubility in water, piperine is typically extracted from black pepper by using organic solvents like dichloromethane. [5] The amount of piperine varies from 1–2% in long pepper, to 5–10% in commercial white and black peppers.

  4. Knoevenagel condensation - Wikipedia

    en.wikipedia.org/wiki/Knoevenagel_condensation

    A Knoevenagel condensation is a nucleophilic addition of an active hydrogen compound to a carbonyl group followed by a dehydration reaction in which a molecule of water is eliminated (hence condensation). The product is often an α,β-unsaturated ketone (a conjugated enone). General Knoevenagel layout

  5. Solvent - Wikipedia

    en.wikipedia.org/wiki/Solvent

    Strongly polar compounds like sugars (e.g. sucrose) or ionic compounds, like inorganic salts (e.g. table salt) dissolve only in very polar solvents like water, while strongly non-polar compounds like oils or waxes dissolve only in very non-polar organic solvents like hexane. Similarly, water and hexane (or vinegar and vegetable oil) are not ...

  6. Hexane - Wikipedia

    en.wikipedia.org/wiki/Hexane

    Hexane (/ ˈ h ɛ k s eɪ n /) or n-hexane is an organic compound, a straight-chain alkane with six carbon atoms and the molecular formula C 6 H 14. [ 7 ] Hexane is a colorless liquid, odorless when pure, and with a boiling point of approximately 69 °C (156 °F).

  7. Pyridine - Wikipedia

    en.wikipedia.org/wiki/Pyridine

    It is a highly flammable, weakly alkaline, water-miscible liquid with a distinctive, unpleasant fish-like smell. Pyridine is colorless, but older or impure samples can appear yellow, due to the formation of extended, unsaturated polymeric chains, which show significant electrical conductivity .

  8. Imine - Wikipedia

    en.wikipedia.org/wiki/Imine

    The reaction of iminophosphoranes and organic azides in an Aza-Wittig-reaction. Condensation of carbon acids with nitroso compounds. The rearrangement of trityl N-haloamines in the Stieglitz rearrangement. By reaction of alkenes with hydrazoic acid in the Schmidt reaction. By reaction of a nitrile, hydrochloric acid, and an arene in the Hoesch ...

  9. N,N'-Dicyclohexylcarbodiimide - Wikipedia

    en.wikipedia.org/wiki/N,N'-Dicyclohexylcarbodiimide

    N,N′-Dicyclohexylcarbodiimide (DCC or DCCD) [1] is an organic compound with the chemical formula (C 6 H 11 N) 2 C. It is a waxy white solid with a sweet odor. Its primary use is to couple amino acids during artificial peptide synthesis.