Date published: 2025-10-14

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1-Adamantanol (CAS 768-95-6)

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Alternate Names:
1-Hydroxyadamantane
CAS Number:
768-95-6
Molecular Weight:
152.23
Molecular Formula:
C10H16O
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-Adamantanol is a compound that functions as a versatile building block in organic synthesis. It serves as a precursor for the preparation of various derivatives, including polymers, and specialty chemicals. Its mechanism of action involves participating in a range of chemical reactions, such as esterification, etherification, and oxidation, to yield structurally diverse products. 1-Adamantanol′s molecular structure allows it to undergo selective functionalization, enabling the creation of new compounds with tailored properties. Its role in the synthesis of complex molecules may be useful for exploring the structure-activity relationships of organic compounds. At the molecular level, 1-Adamantanol′s functional groups facilitate its reactivity, leading to the formation of novel chemical entities with potential applications in various fields of study.


1-Adamantanol (CAS 768-95-6) References

  1. Bioconversion of 1-adamantanol to 1,3-adamantanediol using Streptomyces sp. SA8 oxidation system.  |  Mitsukura, K., et al. 2010. J Biosci Bioeng. 109: 550-3. PMID: 20471592
  2. Supramolecular Control on the Optical Properties of a Dye-Polyelectrolyte Assembly.  |  Awasthi, AA., et al. 2021. Chemphyschem. 22: 975-984. PMID: 33759328
  3. Structural Insights into the Host-Guest Complexation between β-Cyclodextrin and Bio-Conjugatable Adamantane Derivatives.  |  Wang, JW., et al. 2021. Molecules. 26: PMID: 33919170
  4. Covalent cucurbit[7]uril-dye conjugates for sensing in aqueous saline media and biofluids.  |  Hu, C., et al. 2020. Chem Sci. 11: 11142-11153. PMID: 34094355
  5. Rate and Product Studies with 1-Adamantyl Chlorothioformate under Solvolytic Conditions.  |  Park, KH., et al. 2021. Int J Mol Sci. 22: PMID: 34299023
  6. Inhibition of Alkali Metal Reduction of 1-Adamantanol by London Dispersion Effects.  |  Mears, KL., et al. 2022. Angew Chem Int Ed Engl. 61: e202201318. PMID: 35255185
  7. Reviewing a plethora of oxidative-type reactions catalyzed by whole cells of Streptomyces species.  |  Salama, S., et al. 2022. RSC Adv. 12: 6974-7001. PMID: 35424663
  8. Synergistic Brønsted/Lewis acid catalyzed aromatic alkylation with unactivated tertiary alcohols or di-tert-butylperoxide to synthesize quaternary carbon centers.  |  Pan, A., et al. 2022. Chem Sci. 13: 3539-3548. PMID: 35432882
  9. Further Dimensions for Sensing in Biofluids: Distinguishing Bioorganic Analytes by the Salt-Induced Adaptation of a Cucurbit[7]uril-Based Chemosensor.  |  Hu, C., et al. 2022. J Am Chem Soc. 144: 13084-13095. PMID: 35850489
  10. Molecular data storage with zero synthetic effort and simple read-out.  |  Bohn, P., et al. 2022. Sci Rep. 12: 13878. PMID: 35974033
  11. Cucurbit[7]uril Complexation of Near-Infrared Fluorescent Azobenzene-Cyanine Conjugates.  |  Kommidi, SSR. and Smith, BD. 2022. Molecules. 27: PMID: 36080213
  12. Azoarene activation for Schmidt-type reaction and mechanistic insights.  |  Meng, FT., et al. 2022. Nat Commun. 13: 7393. PMID: 36450750
  13. Studies on the nature and pressure evolution of phase transitions in 1-adamantylamine and 1-adamantanol.  |  Jesionek, P., et al. 2023. Spectrochim Acta A Mol Biomol Spectrosc. 299: 122794. PMID: 37167743

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1-Adamantanol, 5 g

sc-253883
5 g
$26.00