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Pyrogallol is an organic compound with the formula C 6 H 3 (OH) 3. It is a water-soluble, white solid although samples are typically brownish because of its sensitivity toward oxygen. [ 3 ] It is one of three isomers of benzenetriols .
Syringol is the organic compound with the formula HO(CH 3 O) 2 C 6 H 3. The molecule is a phenol, with methoxy groups in the flanking (2 and 6) positions. It is the symmetrically dimethylated derivative of pyrogallol. It is a colorless solid, although typical samples are brown owing to air-oxidized impurities.
Phloroglucinol is an organic compound with the formula C 6 H 3 (OH) 3. It is a colorless solid. It is used in the synthesis of pharmaceuticals and explosives. Phloroglucinol is one of three isomeric benzenetriols. The other two isomers are hydroxyquinol (1,2,4-benzenetriol) and pyrogallol (1,2,3-benzenetriol).
Its bulk properties partly result from the interaction of its component atoms, oxygen and hydrogen, with atoms of nearby water molecules. Hydrogen atoms are covalently bonded to oxygen in a water molecule but also have an additional attraction (about 23.3 kJ·mol −1 per hydrogen atom) to an adjacent oxygen atom in a separate molecule. [2]
A hydrolysable tannin or pyrogallol-type tannin is a type of tannin that, on heating with hydrochloric or sulfuric acids, yields gallic or ellagic acids. [ 1 ] At the center of a hydrolysable tannin molecule , there is a carbohydrate (usually D-glucose but also cyclitols like quinic or shikimic acids ).
This enzyme belongs to the family of oxidoreductases, specifically those acting on single donors with O 2 as oxidant and incorporation of two atoms of oxygen into the substrate (oxygenases). The oxygen incorporated need not be derived from O 2. The systematic name of this enzyme class is 1,2,3-trihydroxybenzene:oxygen 1,2-oxidoreductase ...
By reacting the bromopyrogallol red with niobium(V) in a tartrate medium at pH 6.0, an intense blue coloured 3:1 reagent was formed. The sensitivity and conditional selectivity of bromopyrogallol red was also studied and results show that trace amounts of silver can be detected from the formation of a ternary complex between 1,10-phenanthroline, bromopyrogallol red and silver ion.
The reaction can be extended to aliphatic aldehydes with base catalysis in the presence of thiazolium salts; the reaction mechanism is essentially the same. These compounds are important in the synthesis of heterocyclic compounds. The analogous 1,4-addition of an aldehyde to an enone is called the Stetter reaction.