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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.
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 .
3-Methylcatechol; 4-Methylcatechol This page was last edited on 4 February 2015, at 16:22 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4 ...
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]
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.
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.
1.524 g/cm 3 (4 °C) [1] Melting point: ... The enzyme protocatechuate decarboxylase uses 3,4-dihydroxybenzoate to produce catechol and CO 2. The enzyme ...
C 6 H 4 O 2 BH + HC 2 R → C 6 H 4 O 2 B-CHCHR. The product is a precursor to the Suzuki reaction and is the only borane which stops at the alkene instead of reacting further to the alkane. [3] [4] Catecholborane may be used as a stereoselective reducing agent when converting β-hydroxy ketones to syn 1,3-diols.