Date published: 2025-11-3

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Oleyl trifluoromethyl ketone (CAS 177987-23-4)

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CAS Number:
177987-23-4
Molecular Weight:
334.46
Molecular Formula:
C19H33F3O
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Oleyl trifluoromethyl ketone, with the CAS number 177987-23-4, is a specialized chemical compound that blends a long-chain unsaturated oleyl group with a trifluoromethyl ketone functional group. This unique combination imbues the molecule with both hydrophobic and highly electronegative elements, making it an interesting subject for chemical and materials science research. The presence of the trifluoromethyl group adds significant electron-withdrawing character to the molecule, influencing its reactivity and interaction with nucleophilic species. This characteristic is particularly valuable in studies of organofluorine chemistry, where researchers explore the stability, reactivity, and potential applications of fluorinated organic compounds. Oleyl trifluoromethyl ketone′s structure allows it to serve as a surfactant or phase transfer catalyst in various organic reactions, helping to enhance the solubility of organic compounds in aqueous solutions and vice versa. Moreover, the compound′s ability to form stable layers and interfaces is leveraged in creating fluorinated coatings and films, which are notable for their enhanced chemical resistance and low surface energy properties. These attributes are critical in developing advanced materials for coatings that require oil-repellency, water-repellency, or reduced friction. In research, oleyl trifluoromethyl ketone is also used to study lipid bilayers and membrane dynamics, particularly how fluorinated compounds interact with biological and synthetic membranes, impacting their structure and function.


Oleyl trifluoromethyl ketone (CAS 177987-23-4) References

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  7. The discovery and development of inhibitors of fatty acid amide hydrolase (FAAH).  |  Otrubova, K., et al. 2011. Bioorg Med Chem Lett. 21: 4674-85. PMID: 21764305
  8. 2-Amino-5-arylbenzoxazole derivatives as potent inhibitors of fatty acid amide hydrolase (FAAH).  |  Estiarte and M. Angels, et al. 2012. MedChemComm. 3.5: 611-619.
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Oleyl trifluoromethyl ketone, 10 mg

sc-215630
10 mg
$141.00