| Weight | 168.148 g/mol |
|---|---|
| Formula | C8H8O4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
Gallacetophenone (528-21-2, 29477-54-1)
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- Amperometric Determination of Bismuth Using Gallacetophenone Phenylhydrazone with the Structural Elucidation of Complex (Journal of Chemistry, 2010)
- A Rapid and Direct Sensitive Spectrophotometric Method for the Determination of Molybdenum(VI) using Gallacetophenone Phenylhydrazone with Application to Alloy Steel Samples (Journal of Chemistry, 2011)
- UNTOWARD EFFECT OF GALLACETOPHENONE (British Journal of Dermatology, 1892)
- Gallacetophenone as an analytical reagent for tantalum (1973)
- GALLACETOPHENONE OXIME AS A REAGENT FOR GRAVIMETRIC DETERMINATION OF COPPER AND ITS SEPARATION FROM OTHER ELEMENTS. (1971)
- ChemInform Abstract: Aromatic Benzhydrylation. Part 4. Syntheses of Triarylmethane Group of Chalcones, Flavanones, Flavones, Chromones and 2-Methylchromones Using Benzhydrylation of Phloroacetophenone, Gallacetophenone and 5,7-Dihydroxyflavanones. (ChemInform, 1986)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(=O)C1=C(C(=C(C=C1)O)O)O
-
InChIKeyXIROXSOOOAZHLL-UHFFFAOYSA-N
- Pubchem - Gallacetophenone
- Wikipedia - gallacetophenone
Gallacetophenone is the acetyl derivative of pyrogallol. It can be synthesized from pyrogallol using zinc chloride and acetic anhydride.
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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Gallacetophenone
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