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  2. 4-Methylcatechol - Wikipedia

    en.wikipedia.org/wiki/4-methylcatechol

    4-Methyl-1,2-dihydroxybenzene 3,4-Dihydroxytoluene ... 4-Methylcatechol is an organic compound with the formula CH 3 C 6 H 3 (OH) 2 A white solid, ...

  3. Catechol - Wikipedia

    en.wikipedia.org/wiki/Catechol

    Catechol (/ ˈ k æ t ɪ tʃ ɒ l / or / ˈ k æ t ɪ k ɒ l /), also known as pyrocatechol or 1,2-dihydroxybenzene, is an organic compound with the molecular formula C 6 H 4 (OH) 2. It is the ortho isomer of the three isomeric benzenediols .

  4. Piperonal - Wikipedia

    en.wikipedia.org/wiki/Piperonal

    Piperonal can be prepared by the oxidative cleavage of isosafrole or by using a multistep sequence from catechol or 1,2-methylenedioxybenzene.Synthesis from the latter chemical is accomplished through a condensation reaction with glyoxylic acid followed by cleaving the resulting α-hydroxy acid with an oxidizing agent.

  5. Dihydroxybenzenes - Wikipedia

    en.wikipedia.org/wiki/Dihydroxybenzenes

    There are three structural isomers: 1,2-dihydroxybenzene (the ortho isomer) is commonly known as catechol, 1,3-dihydroxybenzene (the meta isomer) is commonly known as resorcinol, and 1,4-dihydroxybenzene (the para isomer) is commonly known as hydroquinone. [1]

  6. p-Cresol - Wikipedia

    en.wikipedia.org/wiki/P-cresol

    ch 3 c 6 h 4 so 3 h + 2 naoh → ch 3 c 6 h 4 oh + na 2 so 3 + h 2 o Other methods for the production of p -cresol include chlorination of toluene followed by hydrolysis. In the cymene-cresol process, toluene is alkylated with propene to give p -cymene , which can be oxidatively dealkylated in a manner similar to the cumene process .

  7. Guaiacol - Wikipedia

    en.wikipedia.org/wiki/Guaiacol

    Guaiacol (/ ˈ ɡ w aɪ ə k ɒ l /) is an organic compound with the formula C 6 H 4 (OH)(OCH 3). It is a phenolic compound containing a methoxy functional group. Guaiacol appears as a viscous colorless oil, although aged or impure samples are often yellowish. It occurs widely in nature and is a common product of the pyrolysis of wood. [3]

  8. Cresol - Wikipedia

    en.wikipedia.org/wiki/Cresol

    Cresols commonly occur as either solids or liquids because their melting points are generally close to room temperature. Like other types of phenols, they are slowly oxidized by exposure to air , and the resulting impurities often give the samples a yellow to brownish red tint.

  9. Melting points of the elements (data page) - Wikipedia

    en.wikipedia.org/wiki/Melting_points_of_the...

    The Gmelin rare earths handbook lists 1522 °C and 1550 °C as two melting points given in the literature, the most recent reference [Handbook on the chemistry and physics of rare earths, vol.12 (1989)] is given with 1529 °C.