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Methyl 9-Formylnonanoate (CAS 14811-73-5)

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Alternate Names:
9-Formylnonanoic Acid Methyl Ester
CAS Number:
14811-73-5
Molecular Weight:
200.28
Molecular Formula:
C11H20O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Methyl 9-Formylnonanoate Acts as a precursor in the synthesis of various organic compounds, contributing to the formation of complex molecular structures. At the molecular level, it participates in esterification reactions, serving as a building block for the creation of more chemical entities. Its mode of action involves undergoing chemical transformations, leading to the generation of novel compounds with potential applications. Methyl 9-Formylnonanoate contributes to the expansion of chemical libraries and the exploration of new chemical space. Its involvement in the creation of diverse chemical structures makes it a component in the development of innovative materials and compounds.


Methyl 9-Formylnonanoate (CAS 14811-73-5) References

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  2. Identification and biosynthesis of (E,E)-10,12-tetradecadienyl acetate in Spodoptera littoralis female sex pheromone gland.  |  Navarro, I., et al. 1997. Bioorg Med Chem. 5: 1267-74. PMID: 9377086
  3. Piperaceae Alkaloids: Part I. Structure of piperstachine; 13C‐and 1H‐NMR. Studies  |  Joshi, B. S., Viswanathan, N., Gawad, D. H., & von Philipsborn, W. 1975. Helvetica Chimica Acta. 58(6): 1551-1559.
  4. Preparation and selective hydrolysis of acetal esters  |  Adlof, R. O., Neff, W. E., Emken, E. A., & Pryde, E. H. 1977. Journal of the American Oil Chemists' Society. 54(10): 414-416.
  5. Isolation, structure and synthesis of maesanin, a host defense stimulant from an African medicinal plant maesalanceolata  |  Kubo, I., Kim, M., Ganjian, I., Kamikawa, T., & Yamagiwa, Y. 1987. Tetrahedron. 43(12): 2653-2660.
  6. An expedient synthesis of the sugarcane borer pheromone components  |  Subbaraman, A. S., Mithran, S., & Mamdapur, V. R. 1998. Molecules. 3(2): 35-40.
  7. One-pot ozonolytic synthesis of acyclic α, ω-bifunctional compounds from methyl 10-undecenoate and 10-undecen-1-ol  |  Legostaeva, Y. V., Botsman, L. P., Nazarov, I. S., Yakovleva, M. P., Garifullina, L. R., Khalikov, R. M., & Ishmuratov, G. Y. 2015. Russian Journal of Applied Chemistry. 88: 935-940.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Methyl 9-Formylnonanoate, 1 g

sc-485803
1 g
$134.00