D107409
2′,4′-Dihydroxyacetophenone
99%
Synonym(s):
1-Acetyl-2,4-dihydroxybenzene, 4-Acetylresorcinol, Resacetophenone
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About This Item
Linear Formula:
(HO)2C6H3COCH3
CAS Number:
Molecular Weight:
152.15
Beilstein:
1282505
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
99%
form
powder
mp
143-144.5 °C (lit.)
density
1.18 g/mL at 25 °C (lit.)
SMILES string
CC(=O)c1ccc(O)cc1O
InChI
1S/C8H8O3/c1-5(9)7-3-2-6(10)4-8(7)11/h2-4,10-11H,1H3
InChI key
SULYEHHGGXARJS-UHFFFAOYSA-N
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Related Categories
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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M C Almandoz et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 77(1), 51-58 (2010-06-16)
The complexation of Al(III) by 2,4(OH)(2)-acetophenone in methanol and ethanol was investigated using spectroscopic methods (UV-vis) and theoretical procedures (DFT) in order to determine its stoichiometry and stability constant and to analyze the effect of temperature, ionic strength and solvent
Hisao Shimizu et al.
Journal of mass spectrometry : JMS, 47(8), 1015-1022 (2012-08-18)
We investigated the application of a high-resolution Orbitrap mass spectrometer equipped with an electrospray ionization (ESI) source and a matrix-assisted laser desorption/ionization-time-of-flight (MALDI-TOF) mass spectrometer to the metabolite profiling of a model small interfering RNA (siRNA) duplex TSR#34 and compared
D J Hopper et al.
The Biochemical journal, 344 Pt 2, 397-402 (1999-11-24)
2,4'-Dihydroxyacetophenone dioxygenase (EC 1.13.11.41) was purified to homogeneity from Alcaligenes sp. 4HAP grown on 4-hydroxyacetophenone. Measurements of the M(r) of the native enzyme ranged from 81600 to 87000, whereas values of 21000 and 20379 were given by SDS/PAGE and electrospray
Xiao-Jun Li et al.
Natural product communications, 6(8), 1129-1130 (2011-09-20)
Biotransformation of paeonol (1) with the white-rot basidiomycete Coriolus versicolor afforded two metabolites, 2,4-dihydroxyacetophenone (2) and 2,5-dihydroxy-4-methoxyacetophenone (3), which were identified by spectroscopic methods. Compound 3 showed higher antioxidative, antibacterial, antifungal activities than 1 or 2. The results demonstrate for
Marek Bunse et al.
Chemistry & biodiversity, 17(4), e1900724-e1900724 (2020-02-26)
The investigations reported here focus on an in-depth characterization of the secondary metabolite profile of Sanguisorba officinalis flowers. For this purpose, fresh flowers were extracted with MeOH/H2 O and EtOH/H2 O and the resulting crude extracts fractionated using CH2 Cl2
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