Date published: 2026-5-8

1-800-457-3801

SCBT Portrait Logo
Seach Input

N-Hydroxy-4-methoxybenzenecarboximidoyl chloride (CAS 38435-51-7)

0.0(0)
Write a reviewAsk a question

CAS Number:
38435-51-7
Molecular Weight:
185.61
Molecular Formula:
C8H8ClNO2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

N-Hydroxy-4-methoxybenzenecarboximidoyl chloride is a compound that functions as a reagent in organic synthesis. It acts as a versatile intermediate in the preparation of various organic compounds, particularly in the formation of amides, esters, and other functional groups. The mechanism of action involves its ability to undergo nucleophilic substitution reactions, allowing for the introduction of the carboximidoyl chloride group into organic molecules. N-Hydroxy-4-Methoxybenzenecarboximidoyl Chloride participates in reactions that lead to the formation of new carbon-nitrogen bonds, contributing to the synthesis of complex organic structures. Its role in the modification of organic molecules may be a useful for the development of novel compounds with potential applications in various fields of research.


N-Hydroxy-4-methoxybenzenecarboximidoyl chloride (CAS 38435-51-7) References

  1. Synthesis, characterization and biological evaluation of some novel 17-isoxazoles in the estrone series.  |  Kovács, D., et al. 2012. Steroids. 77: 1075-85. PMID: 22613036
  2. Synthesis of novel steroidal 16-spiroisoxazolines by 1,3-dipolar cycloaddition, and an evaluation of their antiproliferative activities in vitro.  |  Frank, É., et al. 2014. Mol Divers. 18: 521-34. PMID: 24691697
  3. Regio- and stereoselective access to novel ring-condensed steroidal isoxazolines.  |  Mótyán, G., et al. 2014. Steroids. 87: 76-85. PMID: 24928722
  4. Regio-and stereoselective synthesis of pregnane-fused isoxazolines by nitril-oxide/alkene 1, 3-dipolar cycloaddition and an evaluation of their cell-growth inhibitory effect in vitro  |  Mótyán, G., Baji, Á., Zupkó, I., & Frank, É. 2016. Journal of Molecular Structure. 1110: 143-149.
  5. Microwave-assisted synthesis of (3,5-disubstituted isoxazole)-linked benzimidazolone derivatives: DFT calculations and biological activities  |  Ibrahim, S., Ghabi, A., Amiri, N., Mtiraoui, H., Hajji, M., Bel-Hadj-Tahar, R., & Msaddek, M. 2021. Monatshefte für Chemie-Chemical Monthly. 152(5): 523-535.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

N-Hydroxy-4-methoxybenzenecarboximidoyl chloride, 500 mg

sc-301353
500 mg
$149.00

N-Hydroxy-4-methoxybenzenecarboximidoyl chloride, 1 g

sc-301353A
1 g
$207.00