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  2. 2,4-Dimethoxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/2,4-Dimethoxybenzaldehyde

    2,4-Dimethoxybenzaldehyde (DMBA) is a reagent used to specifically quantify phlorotannins. This product reacts specifically with 1,3-and 1,3,5-substituted phenols (e.g., phlorotannins) to form a colored product. [1]

  3. Lignin peroxidase - Wikipedia

    en.wikipedia.org/wiki/Lignin_peroxidase

    In enzymology, a lignin peroxidase (EC 1.11.1.14) is an enzyme that catalyzes the chemical reaction. 1,2-bis(3,4-dimethoxyphenyl)propane-1,3-diol + H 2 O 2 3,4-dimethoxybenzaldehyde + 1-(3,4-dimethoxyphenyl)ethane-1,2-diol + H 2 O

  4. βk-2C-B - Wikipedia

    en.wikipedia.org/wiki/Βk-2C-B

    Although a synthesis of the compound had previously been described, [2] in the years after its emergence on the market, papers reporting analytical characterizations of the substance appeared. [3] It is offered online and is termed a psychedelic drug. Since 12 October 2016, βk-2C-B has become a controlled substance (Schedule III) in Canada. [4]

  5. DMBA - Wikipedia

    en.wikipedia.org/wiki/DMBA

    2,4-Dimethoxybenzaldehyde, a reagent used to specifically quantify phlorotannins; para-Dimethylaminobenzaldehyde, a reagent used in Ehrlich's reagent and Kovac's reagent; 7,12-Dimethylbenz(a)anthracene, an immunosuppressant and powerful laboratory carcinogen; 1,3-Dimethylbutylamine, a designer stimulant sometimes found in dietary supplements

  6. 3,4,5-Trimethoxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/3,4,5-Trimethoxybenzaldehyde

    3,4,5-Trimethoxybenzaldehyde can be used as an intermediate in the synthesis of some pharmaceutical drugs including trimethoprim, [1] [2] cintriamide, roletamide, trimethoquinol (aka tretoquinol), and trimazosin as well as some psychedelic phenethylamines. [3] [4] [5]

  7. Dimethoxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Dimethoxybenzaldehyde

    Dimethoxybenzaldehyde may refer to: 2,4-Dimethoxybenzaldehyde (DMBA) 2,5-Dimethoxybenzaldehyde; Veratraldehyde (3,4-dimethoxybenzaldehyde) This page was last edited ...

  8. Henry reaction - Wikipedia

    en.wikipedia.org/wiki/Henry_reaction

    The Henry reaction is a classic carbon–carbon bond formation reaction in organic chemistry. Discovered in 1895 by the Belgian chemist Louis Henry (1834–1913), it is the combination of a nitroalkane and an aldehyde or ketone in the presence of a base to form β-nitro alcohols.

  9. 2,4-Dihydroxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/2,4-Dihydroxybenzaldehyde

    2,4-Dihydroxybenzaldehyde or β-resorcylaldehyde is a phenolic aldehyde, a chemical compound with the formula C 7 H 6 O 3. It is an isomer of protocatechuic aldehyde (3,4-dihydroxybenzaldehyde). References