| Weight | 267.835 g/mol |
|---|---|
| Formula | CH2I2 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
DIIODOMETHANE (75-11-6)
methylene iodide · diiodoethane · methylene diiodide
Score:
#1877 in Physics
,
#5841 in Chemistry
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- Synthesis of cyclopropanes by the reaction of olefins with dialkylzinc and methylene iodide (Tetrahedron, 1968)
- Dimethyl(methylene)ammonium Iodide (Angewandte Chemie, 1971)
- New particle formation from photooxidation of diiodomethane (CH2I2) (Journal of Geophysical Research, 2003)
- Cyclopropane Synthesis from Methylene Iodide, Zinc-Copper Couple, and Olefins. III. The Methylene-Transfer Reaction (Journal of the American Chemical Society, 1964)
- Laboratory production of bromoform, methylene bromide, and methyl iodide by macroalgae and distribution in nearshore southern California waters (Limnology and Oceanography, 1992)
- Cyclopropane Synthesis from Methylene Iodide, Zinc-Copper Couple, and Olefins. II.1 Nature of the Intermediate (Journal of the American Chemical Society, 1964)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - methylene iodide
- diiodoethane
- methylene diiodide
- methylene iodide, 14C-labeled
-
SMILESC(I)I
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InChIKeyNZZFYRREKKOMAT-UHFFFAOYSA-N
- Pubchem - DIIODOMETHANE
- Wikipedia - methylene iodide
Diiodomethane or methylene iodide, commonly abbreviated "MI", is an organoiodine compound. Diiodomethane is a colorless liquid; however, it decomposes upon exposure to light liberating iodine, which colours samples brownish. It is slightly soluble in water, but soluble in organic solvents.
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DIIODOMETHANE
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