Atomfair Gallacetophenone C8H8O4

Description Gallacetophenone (CAS 528-21-2) is a high-purity organic compound with the molecular formula C8H8O4and IUPAC name 1-(2,3,4-trihydroxyphenyl)ethanone . This fine chemical is characterized by its trihydroxy-substituted acetophenone structure, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. Gallacetophenone is supplied as an off-white to light brown crystalline powder with a typical purity of ??95% (HPLC). It is soluble in polar organic solvents such as ethanol, methanol, and DMSO, but has limited solubility in water. Suitable for research and development purposes, this compound should be stored in a cool, dry place protected from light to ensure long-term stability.…

Description

Gallacetophenone (CAS 528-21-2) is a high-purity organic compound with the molecular formula C₈H₈O₄ and IUPAC name 1-(2,3,4-trihydroxyphenyl)ethanone. This fine chemical is characterized by its trihydroxy-substituted acetophenone structure, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. Gallacetophenone is supplied as an off-white to light brown crystalline powder with a typical purity of ??95% (HPLC). It is soluble in polar organic solvents such as ethanol, methanol, and DMSO, but has limited solubility in water. Suitable for research and development purposes, this compound should be stored in a cool, dry place protected from light to ensure long-term stability. Available in convenient packaging options from grams to kilograms to meet your laboratory needs.

CAS No: 528-21-2
Molecular Formula: C8H8O4
Molecular Weight: 168.15
Exact Mass: 168.04225873
Monoisotopic Mass: 168.04225873
IUPAC Name: 1-(2,3,4-trihydroxyphenyl)ethanone
SMILES: CC(=O)C1=C(C(=C(C=C1)O)O)O
Synonyms: Gallacetophenone, 528-21-2, 1-(2,3,4-Trihydroxyphenyl)ethanone, 2′,3′,4′-TRIHYDROXYACETOPHENONE, Galloacetophenone

Application

Gallacetophenone serves as a key synthetic intermediate in the preparation of pharmaceutical compounds and specialty chemicals. Researchers utilize this compound in studies of polyphenolic chemistry and as a building block for flavonoid derivatives. Its trihydroxy structure makes it of particular interest in antioxidant research and the development of bioactive molecules. The compound has also found use in biochemical studies of enzyme inhibition and as a reference standard in analytical chemistry.

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