| Weight | 281.862 g/mol |
|---|---|
| Formula | C2H4I2 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
1,2-DIIODOETHANE (624-73-7)
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- Rotational isomerism: V. A nuclear magnetic resonance study of 1,2-diiodoethane (Journal of Molecular Structure, 1969)
- Photodissociation Reaction of 1,2-Diiodoethane in Solution: A Theoretical and X-ray Diffraction Study (Journal of Physical Chemistry A, 2005)
- Structural Dynamics of 1,2-Diiodoethane in Cyclohexane Probed by Picosecond X-ray Liquidography (Journal of Physical Chemistry A, 2012)
- Vibrational frequencies, infrared absorption intensities and energy difference of rotational isomers of 1,2-diiodoethane (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 1974)
- The enthalpies of formation of iodoethane, 1,2-diiodoethane, 1,3-diiodopropane, and 1,4-diiodobutane (The Journal of Chemical Thermodynamics, 1994)
- A-band resonance Raman spectra of 1,2-diiodoethane in cyclohexane solution.: Substituent effects on the 1-halo-2-iodoethane short-time photodissociation dynamics (Chemical Physics Letters, 1998)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESC(CI)I
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InChIKeyGBBZLMLLFVFKJM-UHFFFAOYSA-N
- Pubchem - 1,2-DIIODOETHANE
- Wikipedia - 1,2-Diiodoethane
1,2-Diiodoethane is an organoiodine compound. It is most commonly used in organic synthesis in the preparation of Samarium (II) Iodide or Ytterbium (II) Iodide in THF. S m + I C H 2 C H 2 I T H F S m I 2 + H 2 C = C H 2 {\displaystyle \mathrm {Sm\ +\ ICH_{2}CH_{2}I\ {\xrightarrow[{}]{THF}}\ SmI_{2}\ +\ H_{2}C{=}CH_{2}} }
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