Date published: 2025-10-11

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Exalamide (CAS 53370-90-4)

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Application:
Exalamide is an antifungal agent
CAS Number:
53370-90-4
Purity:
≥99%
Molecular Weight:
221.30
Molecular Formula:
C13H19NO2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Exalamide, a chemical compound that belongs to the class of organic molecules known as amides, specifically designed to engage in non-medical applications such as chemical synthesis and material science. Its structure features an amide linkage, which imparts distinctive chemical properties including stability and reactivity essential for polymer synthesis and modifications. In research settings, exalamide has been explored primarily for its role as a precursor in the production of more complex chemical structures, where it acts as a linking agent facilitating the formation of polymers or enhancing the properties of existing materials. Key to its mechanism of action is its ability to engage in condensation reactions, where it forms covalent bonds with other molecular entities, thereby altering molecular architecture and influencing the physical properties of the resultant materials. Such attributes are invaluable in the development of new materials with improved thermal stability, resistance to degradation, or specific mechanical characteristics. Through these applications, exalamide contributes to advancements in areas such as nanotechnology, coating formulations, and the engineering of specialty plastics, providing insights into the interactions at the molecular level that govern the performance and functionality of synthetic materials.


Exalamide (CAS 53370-90-4) References

  1. Matrix metallopeptidase 9 as a host protein target of chloroquine and melatonin for immunoregulation in COVID-19: A network-based meta-analysis.  |  Hazra, S., et al. 2020. Life Sci. 257: 118096. PMID: 32679150
  2. Comparison of the in vitro antifungal activities of clotrimazole, miconazole, econazole and exalamide against clinical isolates of dermatophytes.  |  Kusunoki, T. and Harada, S. 1984. J Dermatol. 11: 277-81. PMID: 6386917
  3. Prediction of antifungal activity by support vector machine approach.  |  Chen, Shi-Wei, et al. 2005. Journal of molecular structure: THEOCHEM. 731.1-3: 73-81.
  4. Metal-free one-pot oxidative conversion of benzylic alcohols and benzylic halides into aromatic amides with molecular iodine in aq ammonia, and hydrogen peroxide.  |  Ohmura, et al. 2010. Tetrahedron Letters. 51.33: 4378-4381.
  5. Synthesis of primary amides by aminocarbonylation of aryl/hetero halides using non-gaseous NH3 and CO sources.  |  Suresh, A. S., et al. 2015. Tetrahedron letters. 56.34: 4864-4867.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Exalamide, 100 mg

sc-211496
100 mg
$167.00