Date published: 2025-9-27

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1,5-Hexadien-3-ol (CAS 924-41-4)

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Alternate Names:
Hexa-1,5-dien-3-ol
Application:
1,5-Hexadien-3-ol is a compound used in synthesis
CAS Number:
924-41-4
Molecular Weight:
98.14
Molecular Formula:
C6H10O
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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1,5-Hexadien-3-ol is a compound used in synthesis of (+)-obtusenyne and as a reagent for the enantioselective synthesis of (+)-rogioloxepane A. 1,5-Hexadien-3-ol is a naturally occurring monoterpenoid alcohol present in numerous plant spefccies like mint, lavender, and basil. Its significance lies in serving as an intermediate in the biosynthesis of essential oils and other important compounds. This versatile compound plays a key role in various fragrances and finds use in the production of perfumes, soaps, and detergents. Scientists have harnessed its potential to delve into the structure and function of enzymes engaged in essential oil biosynthesis, as well as to investigate the biochemical and physiological effects of these oils on cells.


1,5-Hexadien-3-ol (CAS 924-41-4) References

  1. The anionic oxy-Cope rearrangement: using chemical reactivity to reveal the facile isomerization of the parent substrates in the gas phase.  |  Schulze, SM., et al. 2001. J Org Chem. 66: 7247-53. PMID: 11681934
  2. Enantioselective total synthesis of (+)-rogioloxepane A.  |  Crimmins, MT. and DeBaillie, AC. 2003. Org Lett. 5: 3009-11. PMID: 12916968
  3. Regioselective cross-metathesis reaction induced by steric hindrance.  |  BouzBouz, S., et al. 2004. Org Lett. 6: 3465-7. PMID: 15387524
  4. Chemical composition and biological activities of trans-Himalayan alga Spirogyra porticalis (Muell.) Cleve.  |  Kumar, J., et al. 2015. PLoS One. 10: e0118255. PMID: 25693168
  5. Establishing the volatile profile of pig carcasses as analogues for human decomposition during the early postmortem period.  |  Armstrong, P., et al. 2016. Heliyon. 2: e00070. PMID: 27441249
  6. GC-MS Phytochemical Profiling, Pharmacological Properties, and In Silico Studies of Chukrasia velutina Leaves: A Novel Source for Bioactive Agents.  |  Jahan, I., et al. 2020. Molecules. 25: PMID: 32748850
  7. Shortest Enantioselective Total Syntheses of (+)-Isolaurepinnacin and (+)-Neoisoprelaurefucin.  |  Sinka, V., et al. 2022. Org Lett. 24: 5271-5275. PMID: 35834432
  8. Determination of Reactive Oxygen or Nitrogen Species and Novel Volatile Organic Compounds in the Defense Responses of Tomato Plants against Botrytis cinerea Induced by Trichoderma virens TRS 106.  |  Nawrocka, J., et al. 2022. Cells. 11: PMID: 36231012

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1,5-Hexadien-3-ol, 1 g

sc-223089
1 g
$116.00

1,5-Hexadien-3-ol, 10 g

sc-223089A
10 g
$999.00