Date published: 2025-11-20

1-800-457-3801

SCBT Portrait Logo
Seach Input

(1R)-endo-(+)-Fenchyl alcohol (CAS 2217-02-9)

0.0(0)
Write a reviewAsk a question

Alternate Names:
(+)-Fenchol
CAS Number:
2217-02-9
Molecular Weight:
154.25
Molecular Formula:
C10H18O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

(1R)-endo-(+)-Fenchyl alcohol is an organic compound used in various research applications, particularly in the field of organic synthesis and chiral resolution studies. It serves as a chiral building block for the synthesis of more complex organic molecules, where its stereochemistry is pivotal in the development of enantiomerically pure substances. In synthetic chemistry, researchers utilize (1R)-endo-(+)-Fenchyl alcohol to study asymmetric synthesis methods, exploring its potential to induce chirality in target molecules. Additionally, it is used in the preparation of chiral derivatives and intermediates that are relevant in the synthesis of natural products and potential new compounds. Its role in the investigation of organocatalytic reactions is also significant, where (1R)-endo-(+)-Fenchyl alcohol may act as a starting material or catalyst in promoting stereoselective transformations.


(1R)-endo-(+)-Fenchyl alcohol (CAS 2217-02-9) References

  1. Union of capillary high-performance liquid chromatography and microcoil nuclear magnetic resonance spectroscopy applied to the separation and identification of terpenoids.  |  Lacey, ME., et al. 2001. J Chromatogr A. 922: 139-49. PMID: 11486859
  2. Asymmetric Conversion of Arenechromium Complexes to Functionalized Cyclohexenones: Progress toward Defining an Optimum Chiral Auxiliary.  |  Pearson, AJ. and Gontcharov, AV. 1998. J Org Chem. 63: 152-162. PMID: 11674056
  3. (S)-2-chloro-2-fluoroethanoyl isocyanate, a chiral derivative of trichloroacetyl isocyanate.  |  Vodicka, P., et al. 2003. Chirality. 15: 472-8. PMID: 12692894
  4. Analysis of terpenes and turpentines using gas chromatography with vacuum ultraviolet detection.  |  Qiu, C., et al. 2017. J Sep Sci. 40: 869-877. PMID: 27983761
  5. Volatile components of Rhizoma Alpiniae Officinarum using three different extraction methods combined with gas chromatography-mass spectrometry.  |  Xie, ZS., et al. 2013. J Pharm Anal. 3: 215-220. PMID: 29403820
  6. Extraction of Emerging Contaminants from Environmental Waters and Urine by Dispersive Liquid-Liquid Microextraction with Solidification of the Floating Organic Droplet Using Fenchol:Acetic Acid Deep Eutectic Mixtures.  |  Ortega-Zamora, C., et al. 2022. ACS Sustain Chem Eng. 10: 15714-15725. PMID: 36507093

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

(1R)-endo-(+)-Fenchyl alcohol, 100 g

sc-229842
100 g
$46.00