Date published: 2026-3-13

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Ethyl acetohydroxamate (CAS 10576-12-2)

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Alternate Names:
Ethyl N-hydroxyacetimidate; Ethyl acetohydroximate
Application:
Ethyl acetohydroxamate is a useful chemical for synthesis of O-acyl-and O-nitrophenylhydroxylamines among other chemicals
CAS Number:
10576-12-2
Molecular Weight:
103.12
Molecular Formula:
C4H9NO2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Ethyl acetohydroxamate functions as a chelating agent in experimental applications, binding to metal ions to form stable complexes. Its mechanism of action involves the formation of coordination bonds with metal ions, preventing their participation in various chemical reactions. Ethyl Acetohydroxamate′s functional role includes its ability to inhibit the activity of metal-dependent enzymes by sequestering the metal ions required for their function. Ethyl acetohydroxamate can also be used to remove metal ions from solutions, contributing to the purification of metal-containing compounds in research and development processes. Its mechanism of action involves the formation of stable complexes with metal ions, effectively removing them from the reaction environment. Ethyl Acetohydroxamate′s functional role in experimental applications includes its ability to modulate the reactivity of metal ions, influencing the outcome of chemical reactions and facilitating the isolation of metal-containing compounds for further study.


Ethyl acetohydroxamate (CAS 10576-12-2) References

  1. Metal-free one-pot synthesis of benzofurans.  |  Ghosh, R., et al. 2014. Chemistry. 20: 8888-92. PMID: 24953288
  2. Synthesis of novel chalcones through palladium-catalyzed CO cross-coupling reaction of bromo-chalcones with ethyl acetohydroxamate and their antiplasmodial evaluation against Plasmodium falcipuram in vitro.  |  Reeta, ., et al. 2019. Bioorg Chem. 86: 631-640. PMID: 30818235
  3. Ethyl Acetohydroxamate Incorporated Chalcones: Unveiling a Novel Class of Chalcones for Multitarget Monoamine Oxidase-B Inhibitors Against Alzheimer's Disease.  |  Reeta, ., et al. 2019. CNS Neurol Disord Drug Targets. 18: 643-654. PMID: 31550216
  4. Bioassay-guided isolation and identification of anti-ulcer ecdysteroids from the seeds of Sphenocentrum jollyanum Pierre (Menispermaceae).  |  Akinwumi, IA., et al. 2020. Steroids. 159: 108636. PMID: 32165210
  5. Synthesis and Identification of New N,N-Disubstituted Thiourea, and Thiazolidinone Scaffolds Based on Quinolone Moiety as Urease Inhibitor.  |  Elshaier, YAMM., et al. 2022. Molecules. 27: PMID: 36296723

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Ethyl acetohydroxamate, 10 g

sc-255159
10 g
$98.00