Weight | 169.949 g/mol |
---|---|
Formula | C2H3IO |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
ACETYL IODIDE (507-02-8)
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- Dynamics of threebody half collisions. I. Secondary product decomposition in the photodissociation of acetyl iodide (Journal of Chemical Physics, 1977)
- Reaction of iodocarbonylrhodium ions with methyl iodide. Structure of the rhodium acetyl complex: [Me3PhN+]2[Rh2I6(MeCO)2(CO)2]2 (Journal of Organometallic Chemistry, 1974)
- Synthesis, characterization, stability, aqueous surface activity, and aqueous solution aggregation of the novel, cationic siloxane surfactants (Me3SiO)2Si(Me)-(CH2)3+NMe2(CH2)2OR X- (R = hydrogen, acetyl, N-phenylcarbamyl; X = chloride, bromide, iodide, nitrate, methyl sulfate) (Langmuir, 1993)
- Synthesis and Properties of 2-Acetyl-3,4-dimethylthiazolium Iodide (Journal of the American Chemical Society, 1962)
- Time-resolved and steady-state fluorescence quenching of N-acetyl-L-tryptophanamide by acrylamide and iodide. (Biophysical Chemistry, 1998)
- Displacement Reactions on 2-Acetyl-3,4-dimethylthiazolium Iodide (Journal of the American Chemical Society, 1966)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(=O)I
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InChIKeyLEKJTGQWLAUGQA-UHFFFAOYSA-N
- Pubchem - ACETYL IODIDE
- Wikipedia - acetyl iodide
Acetyl iodide is an organoiodine compound with the formula CH3C(O)I. It is a colourless liquid. It is formally derived from acetic acid.
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