Английская Википедия:Cyclododecanone

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Версия от 12:06, 23 февраля 2024; EducationBot (обсуждение | вклад) (Новая страница: «{{Английская Википедия/Панель перехода}} {{Chembox | ImageFile = Cyclododecanon.png | ImageSize = | ImageAlt = | PIN = Cyclododecanone | OtherNames = |Section1={{Chembox Identifiers | CASNo = 830-13-7 | CASNo_Ref = {{cascite|correct|CAS}} | UNII = WL053118A9 | UNII_Ref = {{fdacite|correct|FDA}} | PubChem = 13246 | ChemSpiderID = 12690 | SMILES = C1CCCCCC(=O)CCCCC1 | StdInChI = 1S/C12H22O/c13-12-10-8-6-4-2-1-3-5-7-9-11-...»)
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Шаблон:Chembox

Cyclododecanone is an organic compound with the formula (CH2)11CO. It is a cyclic ketone that exists as a white solid at room temperature.

Synthesis

It is produced by the oxidation of cyclododecane via cyclododecanol.[1]

Uses

  • Cyclododecanone is mainly consumed as a precursor to 1,12-dodecanedioic acid and laurolactam, which are precursors to certain specialized nylons.
  • Small amounts are also converted to cyclohexadecanone, which is used in some fragrances.[2]

Drug Use

Файл:Swiss cross.svg
Pimagedine-cyclodecanone hydrazone.

Hydrazone formation with pimagedine leads to a hypoglycemic formula.[3] Notice that the shape of the molecule can be made to appear like a pharmacy cross symbol.

References

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Шаблон:Ketone-stub

  1. Schiffer, T.; Oenbrink, G. "Cyclododecanol, Cyclododecanone, and Laurolactam" in Ullman’s Encyclopedia of Industrial Chemistry: Wiley-VCH, 2009. Шаблон:Doi
  2. Johannes Panten and Horst Surburg "Flavors and Fragrances, 2. Aliphatic Compounds" in Ullmann's Encyclopedia of Industrial Chemistry, 2015, Wiley-VCH, Weinheim.Шаблон:Doi
  3. J Nordmann, et al. Шаблон:US patent (1973 to Ugine Kuhlmann SA).