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  1. en.m.wikipedia.org › wiki › Ethyl_iodideEthyl iodide - Wikipedia

    Ethyl iodide (also iodoethane) is a colorless flammable chemical compound. It has the chemical formula C 2 H 5 I and is prepared by heating ethanol with iodine and phosphorus. On contact with air, especially on the effect of light, it decomposes and turns yellow or reddish from dissolved iodine.

  2. Iodoethane is an iodoalkane that is ethane substituted by an iodo group. It derives from a hydride of an ethane.

  3. Oct 25, 2020 · Ethyl iodide or iodoethane is an organic chemical compound of iodine, which appears as a colorless dense liquid (older samples have a brownish or yellowish color), insoluble in water but miscible with other solvents. It has the chemical formula CH3CH2I, sometimes written as EtI .

  4. NIST Mass Spectrometry Data Center, 1994. NIST MS number. 133586. All mass spectra in this site (plus many more) are available from the NIST/EPA/NIH Mass Spectral Library. Please see the following for information about the library and its accompanying search program .

  5. Other names: Ethyl iodide; Hydriodic ether; Iodoethane; Monoiodoethane; C2H5I; Ethyljodid; Jodethan; 1-Iodoethane; NSC 8825 Permanent link for this species. Use this link for bookmarking this species for future reference. Information on this page: Gas phase thermochemistry data; Reaction thermochemistry data; Gas phase ion energetics data; IR ...

  6. Iodoethane; CAS Number: 75-03-6; EC Number: 200-833-1; Synonyms: Ethyl iodide; find Sigma-Aldrich-I4259 MSDS, related peer-reviewed papers, technical documents, similar products & more at Sigma-Aldrich.

  7. Ethyl iodide (also called iodoethane) is a colorless and flammable chemical compound. It has the chemical formula C 2 H 5 I. It is prepared by heating ethanol with iodine and phosphorus

  8. Iodoethane. Synonyms: Ethyl iodide, Iodoethane. Empirical Formula (Hill Notation): C2H5I. CAS Number: 75-03-6. Molecular Weight: 155.97.

  9. Iodoethane. Iodoethane is a chemical compound that refers to the addition of iodide to alkenones using iodotrimethylsilane as a reagent. From: Tetrahedron Organic Chemistry Series, 1992

  10. Reaction thermochemistry data.

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