Molecular structure of 1-Adamantylamine, CAS Number: 768-94-5
1-Adamantylamine (CAS 768-94-5)
Alternate Names:
1-Aminoadamantane
CAS Number:
768-94-5
Purity:
>99%
Molecular Weight:
151.25
Molecular Formula:
C10H17N
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-Adamantylamine is a compound of interest in materials science and organic synthesis due to its bulky adamantane structure, which provides unique steric properties. It is utilized as a building block in the creation of polymers and novel organic materials where rigidity and high thermal stability are desired. Researchers also employ 1-Adamantylamine in the synthesis of dendrimers and other macromolecules that require a well-defined three-dimensional architecture. Its primary amine group allows for straightforward functionalization, enabling the introduction of various substituents to modify the compound′s physical and chemical characteristics. Studies involving 1-Adamantylamine often explore its role in the design of host-guest systems and its interactions with other molecules, which is valuable in the development of new supramolecular assemblies.
1-Adamantylamine (CAS 768-94-5) References
- Cytotoxicity, mutagenicity, cellular uptake, DNA and glutathione interactions of lipophilic trans-platinum complexes tethered to 1-adamantylamine. | Halámiková, A., et al. 2008. J Inorg Biochem. 102: 1077-89. PMID: 18237783
- 1-Adamantylamine a simple urine marker for screening for third generation adamantyl-type synthetic cannabinoids by ultra-performance liquid chromatography tandem mass spectrometry. | Ford, LT. and Berg, JD. 2016. Ann Clin Biochem. 53: 640-646. PMID: 26748105
- Organic Functionalized Graphene Oxide Behavior in Water. | Kim, C., et al. 2020. Nanomaterials (Basel). 10: PMID: 32599799
- Design, synthesis and antimycobacterial evaluation of novel adamantane and adamantanol analogues effective against drug-resistant tuberculosis. | Alsayed, SSR., et al. 2021. Bioorg Chem. 106: 104486. PMID: 33276981
- Facile synthesis and antimycobacterial activity of isoniazid, pyrazinamide and ciprofloxacin derivatives. | Alsayed, SSR., et al. 2021. Chem Biol Drug Des. 97: 1137-1150. PMID: 33638304
- Synthesis and antitumour evaluation of indole-2-carboxamides against paediatric brain cancer cells. | Alsayed, SSR., et al. 2021. RSC Med Chem. 12: 1910-1925. PMID: 34825187
- Spectroscopic study of L-DOPA and dopamine binding on novel gold nanoparticles towards more efficient drug-delivery system for Parkinson's disease. | Kalčec, N., et al. 2022. Spectrochim Acta A Mol Biomol Spectrosc. 268: 120707. PMID: 34902692
- Immuno-affinitive supramolecular magnetic nanoparticles incorporating cucurbit[8]uril-mediated ternary host-guest complexation structures for high-efficient small extracellular vesicle enrichment. | Zhu, N., et al. 2022. J Colloid Interface Sci. 611: 462-471. PMID: 34968965
- Size compatibility and concentration dependent supramolecular host-guest interactions at interfaces. | Park, J., et al. 2022. Nat Commun. 13: 112. PMID: 35013244
- A Polyanionic Strategy to Modify the Perovskite Grain Boundary for a Larger Switching Ratio in Flexible Woven Resistive Random-Access Memories. | Shen, J., et al. 2022. ACS Appl Mater Interfaces. 14: 44652-44664. PMID: 36125291
- Quantum DFT methods to explore the interaction of 1-Adamantylamine with pristine, and P, As, Al, and Ga doped BN nanotubes. | Nemati-Kande, E., et al. 2022. Sci Rep. 12: 19972. PMID: 36402905
- Direct Activation of the C(sp3)-NH2 Bond of Primary Aliphatic Alkylamines by a High-Valent CoIII,IV2(μ-O)2 Diamond Core Complex. | Li, Y., et al. 2023. J Am Chem Soc. 145: 2690-2697. PMID: 36689463
- 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
Inhibitor of:
4930564B18Rik, Adenovirus-1 hexon E11, BDV, CDV, CHRFAM7A, CMV gH, Cngb1, ERICH1, FAM194B, Fv1, GluR-δ1, GRIN2, GRINA, Hep B preS1, IFITM10, Influenza A m1, Influenza A m2, Influenza A NP, Influenza A ns1, Influenza A ns2, Influenza A pb1, Influenza B NA, ISG20, La Crosse Virus G1, LCMV, LEP503, Measles H, Measles M, Measles virus, mGluR-6, Mumps, Mumps NP, Muted, Mx1, N-methyl-D-aspartate (NMDA; GRIN) receptor, NMDA, NMDA zeta 1, OCT, Oct-2, Olfr827, OR2W3, Rabies Virus, RABIF, Rit2, rotavirus vp7, SLC22A15, Slc22a22, SLC22A24, Slc6a16, TAAR8C, UNQ830, vCCI, VP5, and VSV-G.Activator of:
Bunyavirus, D5DR, EAAT4, Influenza A NP, Influenza A ns2, Influenza A Virus Hemagglutinin, KCNT2, La Crosse Virus G1, Measles NP, Mengo 3DPol, Rotavirus virus p42, Rubella Virus gpE1, Rubella Virus structural glycoprotein, St. Louis encephalitis, and synphilin-1.Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1-Adamantylamine, 1 g | sc-251475 | 1 g | $38.00 | |||
1-Adamantylamine, 25 g | sc-251475A | 25 g | $144.00 |