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  2. Iodoform - Wikipedia

    en.wikipedia.org/wiki/Iodoform

    Iodoform stored in an ampoule. Iodoform (also known as triiodomethane) is the organoiodine compound with the chemical formula C H I 3.It is a pale yellow, crystalline, volatile substance, with a penetrating and distinctive odor (in older chemistry texts, the smell is sometimes referred to as that of hospitals, where the compound is still commonly used) and, analogous to chloroform, sweetish taste.

  3. Trihalomethane - Wikipedia

    en.wikipedia.org/wiki/Trihalomethane

    Trifluoromethane and chlorodifluoromethane are both used as refrigerants. Chlorodifluoromethane is a refrigerant HCFC, or hydrochlorofluorocarbon, while fluoroform is an HFC, or hydrofluorocarbon. Fluoroform is not ozone depleting. Chloroform is a common solvent in organic chemistry.

  4. Iodophor - Wikipedia

    en.wikipedia.org/wiki/Iodophor

    Medical iodophor (Chinese povidone-iodine solution) An iodophor is a preparation containing iodine complexed with a solubilizing agent, such as a surfactant or water-soluble polymers such as povidone (forming povidone-iodine), [1] [2] The result is a water-soluble material that releases free iodine when in solution.

  5. Phosgene - Wikipedia

    en.wikipedia.org/wiki/Phosgene

    This was a problem as carbon tetrachloride is an effective fire suppressant and was formerly in widespread use in fire extinguishers. [15] There are reports of fatalities caused by its use to fight fires in confined spaces. [16] Carbon tetrachloride's generation of phosgene and its own toxicity mean it is no longer used for this purpose. [15]

  6. Haloform reaction - Wikipedia

    en.wikipedia.org/wiki/Haloform_reaction

    In chemistry, the haloform reaction (also referred to as the Lieben haloform reaction) is a chemical reaction in which a haloform (CHX 3, where X is a halogen) is produced by the exhaustive halogenation of an acetyl group (R−C(=O)CH 3, where R can be either a hydrogen atom, an alkyl or an aryl group), in the presence of a base.

  7. Takai olefination - Wikipedia

    en.wikipedia.org/wiki/Takai_olefination

    Prior to the introduction of this chromium-based protocol, olefination reactions generally gave Z alkenes or mixtures of isomers. [1] Similar olefination reactions had been performed using a variety of reagents such as zinc and lead chloride; [5] however, these olefination reactions often lead to the formation of diols—the McMurry reaction—rather than the methylenation or alkylidenation of ...

  8. Diiodomethane - Wikipedia

    en.wikipedia.org/wiki/Diiodomethane

    Because of its high density, diiodomethane is used in the determination of the density of mineral and other solid samples. It can also be used as an optical contact liquid, in conjunction with the gemmological refractometer, for determining the refractive index of certain gemstones. Diiodomethane is a reagent for installing the CH 2 group.

  9. Georges-Simon Serullas - Wikipedia

    en.wikipedia.org/wiki/Georges-Simon_Serullas

    In 1822, Serullas added potassium metal to a solution of iodine in ethanol and water to form potassium formate and iodoform, called in the language of that time hydroiodide of carbon, [1] and used as an antiseptic. He is buried in the Père Lachaise Cemetery (10th division). [2] Tomb of Georges Simon Serullas at Père-Lachaise Cemetery