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  2. 4-Methylcatechol - Wikipedia

    en.wikipedia.org/wiki/4-methylcatechol

    Calone, a derivative of 4-methylcatechol, is known in the fragrance industry as "watermelon ketone" for its distinctive odor. [ 3 ] The brand of low-temperature coke used as a smokeless fuel Coalite obtains homocatechol from ammoniacal liquor by solvent extraction, distillation and crystallisation .

  3. Catechol - Wikipedia

    en.wikipedia.org/wiki/Catechol

    C 6 H 4 (OH) 2 + XCl 2 → C 6 H 4 (O 2 X) + 2 HCl where X = PCl or POCl; SO 2; CO. Basic solutions of catechol react with iron(III) to give the red [Fe(C 6 H 4 O 2) 3] 3−. Ferric chloride gives a green coloration with the aqueous solution, while the alkaline solution rapidly changes to a green and finally to a black color on exposure to the ...

  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. Cresol - Wikipedia

    en.wikipedia.org/wiki/Cresol

    The Occupational Safety and Health Administration has set a permissible exposure limit at 5 ppm (22 mg/m 3) over an eight-hour time-weighted average, while the National Institute for Occupational Safety and Health recommends a limit of 2.3 ppm (10 mg/m 3).

  7. 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 .

  8. 3-Methylcatechol - Wikipedia

    en.wikipedia.org/wiki/3-methylcatechol

    3-Methylcatechol is an organic compound with the formula CH 3 C 6 H 3 (OH) 2 A white solid, it is one of the isomers of methylbenzenediol. Being structurally related to lignans , it is contributes to the aerosol generate by combustion of wood.

  9. 4-tert-Butylcatechol - Wikipedia

    en.wikipedia.org/wiki/4-tert-Butylcatechol

    4-tert-Butylcatechol (TBC) is an organic chemical compound which is a derivative of catechol. [1] TBC is available in the form of a solid crystal flake [ 2 ] and 85% solution in methanol [ 3 ] or water.