Date published: 2025-11-2

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Cyclooctane (CAS 292-64-8)

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CAS Number:
292-64-8
Molecular Weight:
112.21
Molecular Formula:
C8H16
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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Cyclooctane serves as a saturated hydrocarbon and nonpolar solvent. Its utility stems from its ability to engage with nonpolar molecules through London dispersion forces, thereby dissolving them efficiently and fostering a conducive environment for organic reactions. This interaction not only facilitates the dissolution of otherwise insoluble substances but ensures that reactions proceed in a more controlled and uniform manner. As a reaction medium, cyclooctane is instrumental in the synthesis and manipulation of complex organic compounds. It helps maintain the stability and purity of reactive species within a homogeneous solution, thereby optimizing reaction conditions and enhancing yield. The inherent characteristics of cyclooctane, such as its nonpolar nature and chemical inertness, make it indispensable in experimental procedures aimed at exploring reaction dynamics, synthesizing novel compounds, and developing innovative chemical processes.


Cyclooctane (CAS 292-64-8) References

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  2. Metalloradical-catalyzed aliphatic carbon-carbon activation of cyclooctane.  |  Chan, YW. and Chan, KS. 2010. J Am Chem Soc. 132: 6920-2. PMID: 20441175
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  4. Doped graphene as a metal-free carbocatalyst for the selective aerobic oxidation of benzylic hydrocarbons, cyclooctane and styrene.  |  Dhakshinamoorthy, A., et al. 2013. Chemistry. 19: 7547-54. PMID: 23576323
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  7. Efficient gradient calibration based on diffusion MRI.  |  Teh, I., et al. 2017. Magn Reson Med. 77: 170-179. PMID: 26749277
  8. Biocatalytic conversion of cycloalkanes to lactones using an in-vivo cascade in Pseudomonas taiwanensis VLB120.  |  Karande, R., et al. 2018. Biotechnol Bioeng. 115: 312-320. PMID: 28986995
  9. Determining the necessity of phenyl ring π-character in warfarin.  |  Xing, H., et al. 2019. Bioorg Med Chem Lett. 29: 1954-1956. PMID: 31147103
  10. Systematic description of molecular deformations with Cremer-Pople puckering and deformation coordinates utilizing analytic derivatives: Applied to cycloheptane, cyclooctane, and cyclo[18]carbon.  |  Zou, W., et al. 2020. J Chem Phys. 152: 154107. PMID: 32321269
  11. Dimerizing cascades of enallenamides reveal the visible-light-promoted activation of cumulated C-C double bonds.  |  Serafino, A., et al. 2022. Chem Sci. 13: 2632-2639. PMID: 35340858
  12. A Method to Derive Structural Information on Molecules from Residual Dipolar Coupling NMR Data.  |  van Gunsteren, WF., et al. 2022. J Phys Chem B. 126: 3867-3888. PMID: 35588494
  13. Bicyclic Isoxazoline Derivatives: Synthesis and Evaluation of Biological Activity.  |  Sedenkova, KN., et al. 2022. Molecules. 27: PMID: 35684482
  14. Induced Fit and Mobility of Cycloalkanes within Nanometer-Sized Confinements at 5 K.  |  Ahsan, A., et al. 2022. J Phys Chem Lett. 13: 7504-7513. PMID: 35943183
  15. Zirconium-Catalyzed C-H Alumination of Polyolefins, Paraffins, and Methane.  |  Kanbur, U., et al. 2023. J Am Chem Soc. 145: 2901-2910. PMID: 36696148

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Cyclooctane, 1 ml

sc-239616
1 ml
$37.00