Weight | 120.151 g/mol |
---|---|
Formula | C8H8O |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
ACETOPHENONE (98-86-2)
Score:
#424 in Physics
,
#1254 in Chemistry
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- Mechanism of Asymmetric Hydrogenation of Acetophenone Catalyzed by Chiral 6-AreneN-TosylethylenediamineRuthenium(II) Complexes (Chemistry-an Asian Journal, 2006)
- Catalytic behavior of optically active amino alcohol-borane complex in the enantioselective reduction of acetophenone oxime O-alkyl ethers. (Bulletin of the Chemical Society of Japan, 1987)
- Variation of Langmuir adsorption constant determined for TiO2-photocatalyzed degradation of acetophenone under different light intensity (Journal of Photochemistry and Photobiology A-chemistry, 2000)
- Effects of solvent and substituents on the absorption spectra of triplet acetophenone and the acetophenone ketyl radical studied by nanosecond laser photolysis (The Journal of Physical Chemistry, 1973)
- Low-Valent EneAmido Iron Complexes for the Asymmetric Transfer Hydrogenation of Acetophenone without Base (Journal of the American Chemical Society, 2011)
- PMDR studies of the magnetic and dynamic properties of the lowest excited triplet states of aromatic carbonyl molecules : acetophenone, benzaldehyde and their derivatives (Molecular Physics, 1974)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H227: Combustible liquid
Warning Flammable liquids - Category 4 - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H316: Causes mild skin irritation
Warning Skin corrosion/irritation - Category 3 - H336: May cause drowsiness or dizziness
Warning Specific target organ toxicity, single exposure; Narcotic effects - Category 3 -
SMILESCC(=O)C1=CC=CC=C1
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InChIKeyKWOLFJPFCHCOCG-UHFFFAOYSA-N
- Pubchem - ACETOPHENONE
- Wikipedia - acetophenone
Acetophenone is the organic compound with the formula C6H5C(O)CH3 (also represented by the pseudoelement symbols PhAc or BzMe). It is the simplest aromatic ketone. This colorless, viscous liquid is a precursor to useful resins and fragrances.
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