To install click the Add extension button. That's it.

The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. You could also do it yourself at any point in time.

4,5
Kelly Slayton
Congratulations on this excellent venture… what a great idea!
Alexander Grigorievskiy
I use WIKI 2 every day and almost forgot how the original Wikipedia looks like.
Live Statistics
English Articles
Improved in 24 Hours
Added in 24 Hours
Languages
Recent
Show all languages
What we do. Every page goes through several hundred of perfecting techniques; in live mode. Quite the same Wikipedia. Just better.
.
Leo
Newton
Brights
Milds

Cyclododecanone

From Wikipedia, the free encyclopedia

Cyclododecanone
Names
Preferred IUPAC name
Cyclododecanone
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.011.450 Edit this at Wikidata
UNII
  • InChI=1S/C12H22O/c13-12-10-8-6-4-2-1-3-5-7-9-11-12/h1-11H2
    Key: SXVPOSFURRDKBO-UHFFFAOYSA-N
  • C1CCCCCC(=O)CCCCC1
Properties
C12H22O
Molar mass 182.307 g·mol−1
Appearance white solid
Melting point 60.8 °C (141.4 °F; 333.9 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

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

YouTube Encyclopedic

  • 1/2
    Views:
    9 515
    133 577
  • Hypochlorite Oxidation Mechanism - Conversion of alcohols to ketones
  • Hydroboration-oxidation: Mechanism | Alkenes and Alkynes | Organic chemistry | Khan Academy

Transcription

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

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

  1. ^ Schiffer, T.; Oenbrink, G. "Cyclododecanol, Cyclododecanone, and Laurolactam" in Ullman’s Encyclopedia of Industrial Chemistry: Wiley-VCH, 2009. doi:10.1002/14356007.a08_201.pub2
  2. ^ Johannes Panten and Horst Surburg "Flavors and Fragrances, 2. Aliphatic Compounds" in Ullmann's Encyclopedia of Industrial Chemistry, 2015, Wiley-VCH, Weinheim.doi:10.1002/14356007.t11_t01
  3. ^ J Nordmann, et al. U.S. patent 3,746,764 (1973 to Ugine Kuhlmann SA).


This page was last edited on 11 October 2023, at 15:00
Basis of this page is in Wikipedia. Text is available under the CC BY-SA 3.0 Unported License. Non-text media are available under their specified licenses. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc. WIKI 2 is an independent company and has no affiliation with Wikimedia Foundation.