Date published: 2025-9-18

1-800-457-3801

SCBT Portrait Logo
Seach Input

5-Bromo-2-adamantanone (CAS 20098-20-8)

0.0(0)
Write a reviewAsk a question

Alternate Names:
1-Bromoadamantan-4-one
CAS Number:
20098-20-8
Molecular Weight:
229.11
Molecular Formula:
C10H13BrO
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

5-Bromo-2-adamantanone is a cyclic ketone compound. 5-Bromo-2-adamantanone is utilized as a building block in the synthesis of various organic molecules due to its unique structure and reactivity. 5-Bromo-2-adamantanone has ability to undergo nucleophilic substitution reactions, making it valuable in the creation of complex organic compounds. In biochemistry, 5-Bromo-2-adamantanone is frequently used in the development of agrochemicals. Its versatile nature and reactivity make it an component in the study of organic chemistry and the synthesis of biologically active molecules.


5-Bromo-2-adamantanone (CAS 20098-20-8) References

  1. Triorganostannylation of halo- and dihaloadamantanes and 5-chloro-2-adamantanone in liquid ammonia by the S(RN)1 mechanism. Relative reactivity of nucleophiles and bridgehead halides.  |  Santiago, AN., et al. 2002. J Org Chem. 67: 2494-500. PMID: 11950293
  2. Structure-reactivity relationships: reactions of a 5-substituted aziadamantane in a resorcin[4]arene-based cavitand.  |  Wagner, G., et al. 2010. Org Lett. 12: 332-5. PMID: 20017550
  3. Copper-Catalyzed Trifluoromethylation of Alkyl Bromides.  |  Kornfilt, DJP. and MacMillan, DWC. 2019. J Am Chem Soc. 141: 6853-6858. PMID: 30983333
  4. Solvent Selective Effect Occurs in Iodinated Adamantanone Ferroelectrics.  |  Xu, L., et al. 2022. Adv Sci (Weinh). 9: e2201702. PMID: 35470590
  5. Alkyl group stabilization of monoolefin radical cations. ESR, ENDOR, and cyclic voltammetry study  |  Gerson, F., Lopez, J., Akaba, R., & Nelsen, S. F. 1981. Journal of the American Chemical Society. 103(22): 6716-6722.
  6. Novel approach to trisubstituted adamantanes  |  Kovalev, V. V., Rozov, A. K., & Shokova, E. A. 1996. Tetrahedron. 52(11): 3983-3990.
  7. Heteroatom-Substituted Delaminated Zeolites as Solid Lewis Acid Catalysts  |  Ouyang, X., Hwang, S. J., Xie, D., Rea, T., Zones, S. I., & Katz, A. 2015. ACS Catalysis. 5(5): 3108-3119.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

5-Bromo-2-adamantanone, 1 g

sc-226915
1 g
$83.00