Date published: 2026-4-24

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1,3-Dimethyladamantane (CAS 702-79-4)

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CAS Number:
702-79-4
Purity:
≥99%
Molecular Weight:
164.29
Molecular Formula:
C12H20
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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1,3-Dimethyladamantane is a hydrophobic molecule that can act as a nonpolar solvent in various experimental applications. It has the ability to interact with other nonpolar molecules, facilitating the dissolution of certain compounds during experimental procedures. 1,3-Dimethyladamantane can also serve as a stabilizing agent for certain reactions, due to its nonpolar nature and ability to form weak interactions with other molecules. 1,3-Dimethyladamantane can act as a molecular scaffold in the synthesis of certain organic compounds, providing a rigid and stable structure for further chemical modifications. Its unique structure allows it to participate in specific molecular interactions, making it useful in the development of certain experimental protocols. 1,3-Dimethyladamantane plays a functional role in various experimental applications, contributing to the successful execution of certain chemical processes.


1,3-Dimethyladamantane (CAS 702-79-4) References

  1. Catalytic oxyalkylation of alkenes with alkanes and molecular oxygen via a radical process using N-hydroxyphthalimide.  |  Hara, T., et al. 2001. J Org Chem. 66: 6425-31. PMID: 11559195
  2. Remote substituent effects on phenylchlorocarbene C-H insertion reactions.  |  Moss, RA. and Yan, S. 1999. Org Lett. 1: 819-22. PMID: 16118887
  3. Evaluation of the diagnostic ratios of adamantanes for identifying seriously weathered spilled oils from simulated experiment and actual oil spills.  |  Han, B., et al. 2019. Environ Geochem Health. 41: 817-828. PMID: 30225731
  4. A New Process for Production of 1, 3-Dimethyladamantane  |  Takagi, K., & Naruse, Y. 1993. In Studies in Surface Science and Catalysis. 75: 2455-2458.
  5. The low-temperature heat capacities, phase transitions and thermodynamic properties of 1, 3-dimethyladamantane and 1-ethyladamantane  |  Varushchenko, R. M., Druzhinina, A. I., Senyavin, V. M., & Sarkisova, V. S. 2005. The Journal of Chemical Thermodynamics. 37(2): 141-151.
  6. On a possible radical-cation mechanism of the biomimetic oxidation of the saturated hydrocarbon 1, 3-dimethyladamantane in a Gif-type system containing a Fe 2+ salt, picolinic acid, and pyridine  |  Shchapin, I. Y., Vasil'eva, V. V., Nekhaev, A. I., & Bagrii, E. I. 2006. Kinetics and catalysis. 47: 624-637.
  7. The first selective one-pot synthesis of 1, 3-dicarbonyl adamantanes from adamantane and 1, 3-dimethyladamantane  |  Akhrem, I. S., Dzhul'etta, V. A., & Afanas'eva, L. V. 2012. Tetrahedron Letters. 53(27): 3493-3496.
  8. Synthesis of 1,3-dimethyladamantane by skeletal rearrangement of C12H18 and C12H20 hydrocarbons over Na/H-Y-zeolite  |  Khusnutdinov, R. I., Kislitsina, K. S., Khazipova, A. N., & Kutepov, B. I. 2013. Russian Journal of Organic Chemistry. 49: 1273-1278.
  9. Synthesis of 3, 5-dimethyladamantan-1-ol by reaction of 1, 3-dimethyladamantane with bromotrichloromethane and water in the presence of manganese complexes  |  Khusnutdinov, R. I., Kislitsina, K. S., & Shchadneva, N. A. 2014. Russian Journal of Organic Chemistry. 50: 25-28.
  10. Density and viscosity of ternary mixture of cyclopentanol+ exo-tetrahydrodicyclopentadiene+ 1, 3-dimethyladamantane  |  Zhao, L., Ye, D., Guo, Y., & Fang, W. 2019. Journal of Chemical & Engineering Data. 64(6): 2558-2567.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1,3-Dimethyladamantane, 5 g

sc-253982
5 g
$54.00