Search

  • Order Status
  • Quick Order
  • Promos
Ethyl N-hydroxyacetimidate, 97%
Element SearchElement SearchStructure SearchStructure Search
Ethyl N-hydroxyacetimidate, 97%
Ethyl N-hydroxyacetimidate, 97%
Ethyl N-hydroxyacetimidate, 97%
Thermo Scientific Chemicals

Ethyl N-hydroxyacetimidate, 97%

CAS: 10576-12-2 | C4H9NO2 | 103.12 g/mol
Have Questions?
Change viewbuttonViewtableView
Quantity:
5 g
25 g
100 g
ChemDexTry the chem dexTM web app
Catalog number A11006.14
also known as A11006-14
Price (USD)
117.65
Special offer
Online exclusive
Ends: 30-Jun-2026
138.00
Save 20.35 (15%)
Each
Add to cart
Quantity:
25 g
Request bulk or custom format
Price (USD)
117.65
Special offer
Online exclusive
Ends: 30-Jun-2026
138.00
Save 20.35 (15%)
Each
Add to cart
Chemical Identifiers
CAS10576-12-2
IUPAC Name(E)-(ethyl N-hydroxyethanimidate)
Molecular FormulaC4H9NO2
InChI KeyQWKAVVNRCKPKNM-SNAWJCMRSA-N
SMILESCCO\C(C)=N\O
View more
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Colorless to white to pale yellow
FormFused solid or clear liquid as melt
Assay (GC)≥96.0%
Refractive Index1.4315-1.4365 @ 20?C
Ethyl N-hydroxyacetimidate was used in the synthesis of O-acyl-and O-nitrophenylhydroxylamines, hydroxamic acid ethoxycarbonylhydrazides and ethyl O-(2,4-dinitrophenyl)acetohydroxamate.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Ethyl N-hydroxyacetimidate was used in the synthesis of O-acyl-and O-nitrophenylhydroxylamines, hydroxamic acid ethoxycarbonylhydrazides and ethyl O-(2,4-dinitrophenyl)acetohydroxamate.

Solubility
Decompose in water.

Notes
Moisture sensitive. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Gerald A.Rosenthal; Deborah Thomas. Radiochemical synthesis of dl-canaline and the colorimetric assay of canaline. Analytical Biochemistry. 1984, 140,(1), 246-249.
  2. Natalia Shpiro; Rodolfo Marquez. Improved experimental procedure for the synthesis of the potent MEK inhibitor PD184352. Synthetic Communications: An International Journal for Rapid Communication of Synthetic Organic Chemistry. 2005, 35,(17), 2265-2269.