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  2. Catechol - Wikipedia

    en.wikipedia.org/wiki/Catechol

    By 1852, Erdmann realized that catechol was benzene with two oxygen atoms added to it; in 1867, August Kekulé realized that catechol was a diol of benzene, so by 1868, catechol was listed as pyrocatechol. [7] In 1879, the Journal of the Chemical Society recommended that catechol be called "catechol", and in the following year, it was listed as ...

  3. Catecholborane - Wikipedia

    en.wikipedia.org/wiki/Catecholborane

    Unlike borane itself or alkylboranes, catechol borane exists as a monomer. This behavior is a consequence of the electronic influence of the aryloxy groups that diminish the Lewis acidity of the boron centre. Pinacolborane adopts a similar structure.

  4. 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.

  5. Category:Catechols - Wikipedia

    en.wikipedia.org/wiki/Category:Catechols

    Catechol ethers (5 C, 71 P) Catecholamines (5 C, 51 P) Pages in category "Catechols" The following 140 pages are in this category, out of 140 total.

  6. Catechol 1,2-dioxygenase - Wikipedia

    en.wikipedia.org/wiki/Catechol_1,2-dioxygenase

    Figure 1. The overall reaction of catechol 1,2-dioxygenase. Using a non-heme iron(III) complex, 1,2-CTD is able to oxidatively cleave catechol into cis,cis-muconic acid. More specifically, 1,2-CTD is an intradiol dioxygenase, a family of catechol dioxygenases that cleaves the bond between the phenolic hydroxyl groups of catechol using an Fe 3 ...

  7. 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. [4]

  8. Catechol oxidase - Wikipedia

    en.wikipedia.org/wiki/Catechol_oxidase

    As catechol enters the active site, a proton is abstracted from one of the alcohols. The catechol coordinates with a Cu(II) center in a monodentate fashion, displacing one of the coordinating histidine residues. The coordinated hydroxide ion abstracts another proton from catechol to form water, and the catechol is oxidized to o-quinone.

  9. Catecholamine - Wikipedia

    en.wikipedia.org/wiki/Catecholamine

    Catechol. A catecholamine (/ ˌ k æ t ə ˈ k oʊ l ə m iː n /; abbreviated CA) is a monoamine neurotransmitter, an organic compound that has a catechol (benzene with two hydroxyl side groups next to each other) and a side-chain amine. [1] Catechol can be either a free molecule or a substituent of a larger molecule, where it represents a 1,2 ...