Gallacetophenone

Last updated
Gallacetophenone
Gallacetophenone.svg
Names
Preferred IUPAC name
1-(2,3,4-Trihydroxyphenyl)ethan-1-one
Other names
1-(2,3,4-Trihydroxyphenyl)ethanone
Alizarin Yellow C
Galloacetophenone
2',3',4'-Trihydroxyacetophenone
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.007.665
PubChem CID
UNII
Properties
C8H8O4
Molar mass 168.148 g·mol−1
Melting point 171 to 172 °C (340 to 342 °F; 444 to 445 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Gallacetophenone is the acetyl derivative of pyrogallol. It can be synthesized from pyrogallol using zinc chloride and acetic anhydride. [1]

Related Research Articles

Polyphenol Class of chemical compounds

Polyphenols are a structural class of mainly natural, but also synthetic or semisynthetic, organic chemicals characterized by the presence of large multiples of phenol structural units. The number and characteristics of these phenol structures underlie the unique physical, chemical, and biological properties of particular members of the class. Examples include tannic acid and ellagitannin. The historically important chemical class of tannins is a subset of the polyphenols.

A calixarene is a macrocycle or cyclic oligomer based on a hydroxyalkylation product of a phenol and an aldehyde.

Phloroglucinol chemical compound

Phloroglucinol is an organic compound with the formula C6H3(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). Phloroglucinol, and its benzenetriol isomers, are still defined as "phenols" according to the IUPAC official nomenclature rules of chemical compounds. Many such monophenolics are often termed "polyphenols" by the cosmetic and parapharmaceutical industries, which does not match the scientifically accepted definition.

Pyrogallol chemical compound

Pyrogallol is an organic compound with the formula C6H3(OH)3. It is a white, water-soluble solid although samples are typically brownish because of its sensitivity toward oxygen. It is one of three isomeric benzenetriols.

Dakin oxidation organic redox reaction in which an ortho- or para-hydroxylated phenyl aldehyde or ketone reacts with hydrogen peroxide in base to form a benzenediol and a carboxylate

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A resorcinarene is a macrocycle, or a cyclic oligomer, based on the condensation of resorcinol (1,3-dihydroxybenzene) and an aldehyde. Resorcinarenes are a type of calixarene. Other types of resorcinarenes include the related pyrogallolarenes and octahydroxypyridines, derived from pyrogallol and 2,6-dihydroxypyridine, respectively.

Picamar is a colorless, hydrocarbon oil extracted from the creosote of beechwood tar with a peculiar odor and bitter taste. It consists of derivatives of pyrogallol. It was discovered by German chemist Karl von Reichenbach in the 1830s.

Sulfolene chemical compound

Sulfolene, or butadiene sulfone is a cyclic organic chemical with a sulfone functional group. It is a white, odorless, crystalline, indefinitely storable solid, which dissolves in water and many organic solvents. The compound is used as a source of butadiene.

In enzymology, a pyrogallol hydroxytransferase is an enzyme that catalyzes the chemical reaction

In enzymology, a pyrogallol 1,2-oxygenase (EC 1.13.11.35) is an enzyme that catalyzes the chemical reaction

In enzymology, a gallate decarboxylase (EC 4.1.1.59) is an enzyme that catalyzes the chemical reaction

Trihydroxyacetophenone may refer to

Syringic acid chemical compound

Syringic acid is a naturally occurring phenolic compound and dimethoxybenzene that is commonly found as a plant metabolite.

Mesquitol chemical compound

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Trihydroxybenzenes group of isomers

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1,2,3,5-Tetrahydroxybenzene chemical compound

1,2,3,5-Tetrahydroxybenzene is a benzenetetrol.

Alizarine yellow may refer to:

Bismuth(III) nitrate chemical compound

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Colin Llewellyn Raston is a Professor of Chemistry of Flinders University in Adelaide, South Australia and the Premier's Professorial Fellow in Clean Technology. In 2015, he was awarded an Ig Nobel Prize in "for inventing a chemical recipe to partially un-boil an egg." In 2016, Raston was made an Officer of the Order of Australia for his services to science.

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