| Weight | 152.149 g/mol |
|---|---|
| Formula | C8H8O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2',6'-Dihydroxyacetophenone (699-83-2)
dihydroxyacetophenone · 2,6-dihydroxyacetophenone
Score:
#2010 in Biochemistry
,
#5319 in Chemistry
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- Use of 2,6Dihydroxyacetophenone for Analysis of Fragile Peptides, Disulphide Bonding and Small Proteins by Matrixassisted Laser Desorption/Ionization (Rapid Communications in Mass Spectrometry, 1996)
- Isolation of arterenone (2-amino-3,4-dihydroxyacetophenone) from hydrolysates of scleratized insect cuticle (Journal of Insect Physiology, 1970)
- MATRIX-ASSISTED LASER DESORPTION/IONIZATION TIME-OF-FLIGHT MASS SPECTROMETRY OF SIALYLATED GLYCOPEPTIDES AND PROTEINS USING 2,6-DIHYDROXYACETOPHENONE AS A MATRIX (Rapid Communications in Mass Spectrometry, 1996)
- Antimelanogenic Activity of 3,4-Dihydroxyacetophenone : Inhibition of Tyrosinase and MITF (Bioscience, Biotechnology, and Biochemistry, 2006)
- Theoretical and practical investigations of copper ion selective electrode with polymeric membrane based on N,N-(2,2-dimethylpropane-1,3-diyl)-bis(dihydroxyacetophenone) (Electrochimica Acta, 2011)
- Monomeric and dimeric copper(II) complexes of a redox active Schiff base ligand bis(2,5-dihydroxyacetophenone) ethylenediamine (Polyhedron, 1994)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - dihydroxyacetophenone
- 2,6-dihydroxyacetophenone
-
SMILESCC(=O)C1=C(C=CC=C1O)O
-
InChIKeyYPTJKHVBDCRKNF-UHFFFAOYSA-N
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Alternate Names
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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(394-32-1)
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2',6'-Dihydroxyacetophenone
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