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  2. Pyrogallol - Wikipedia

    en.wikipedia.org/wiki/Pyrogallol

    Pyrogallol is an organic compound with the formula C 6 H 3 (OH) 3. It is a water-soluble, white solid although samples are typically brownish because of its sensitivity toward oxygen. [ 3 ] It is one of three isomers of benzenetriols .

  3. Pyrogallolarenes - Wikipedia

    en.wikipedia.org/wiki/Pyrogallolarenes

    A pyrogallolarene (also calix[4]pyrogallolarene) is a macrocycle, or a cyclic oligomer, based on the condensation of pyrogallol (1,2,3-trihydroxybenzene) and an aldehyde. Pyrogallolarenes are a type of calixarene , and a subset of resorcinarenes that are substituted with a hydroxyl at the 2-position.

  4. Syringol - Wikipedia

    en.wikipedia.org/wiki/Syringol

    It is the symmetrically dimethylated derivative of pyrogallol. It is a colorless solid, although typical samples are brown owing to air-oxidized impurities. Together with guaiacol, syringol and its derivatives are produced by the pyrolysis of lignin. Specifically, syringol is derived from the thermal decomposition of the sinapyl alcohol component.

  5. Hydrolysable tannin - Wikipedia

    en.wikipedia.org/wiki/Hydrolysable_tannin

    A hydrolysable tannin or pyrogallol-type tannin is a type of tannin that, on heating with hydrochloric or sulfuric acids, yields gallic or ellagic acids. [ 1 ] At the center of a hydrolysable tannin molecule , there is a carbohydrate (usually D-glucose but also cyclitols like quinic or shikimic acids ).

  6. Resorcinarene - Wikipedia

    en.wikipedia.org/wiki/Resorcinarene

    1 Synthesis. 2 Structure. 3 Catalysis. ... a resorcinarene (also resorcarene or calix[4]resorcinarene) is a macrocycle, ... derived from pyrogallol and 2,6 ...

  7. Phloroglucinol - Wikipedia

    en.wikipedia.org/wiki/Phloroglucinol

    It is a colorless solid. It is used in the synthesis of pharmaceuticals and explosives. Phloroglucinol is one of three isomeric benzenetriols. The other two isomers are hydroxyquinol (1,2,4-benzenetriol) and pyrogallol (1,2,3-benzenetriol).

  8. Sulfolene - Wikipedia

    en.wikipedia.org/wiki/Sulfolene

    Synthesis of sulfolene. Sulfolene is formed by the cheletropic reaction between butadiene and sulfur dioxide. The reaction is typically conducted in an autoclave. Small amounts of hydroquinone or pyrogallol are added to inhibit polymerization of the diene. The reaction proceeds at room temperature over the course of days.

  9. Calixarene - Wikipedia

    en.wikipedia.org/wiki/Calixarene

    With finely tuned starting materials and reaction conditions, synthesis can also be surprisingly efficient. Calixarenes are sparingly soluble as parent compounds and have high melting points. [8] from left to right with n = 4 calix[4]arene, resorcinol[4]arene, pyrogallol[4]arene.