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Thermo Scientific Chemicals
Ethyl N-hydroxyacetimidate, 97%
CAS: 10576-12-2 | C4H9NO2 | 103.12 g/mol
化学物質識別子
CAS10576-12-2
IUPAC Name(E)-(ethyl N-hydroxyethanimidate)
Molecular FormulaC4H9NO2
InChI KeyQWKAVVNRCKPKNM-SNAWJCMRSA-N
SMILESCCO\C(C)=N\O
さらに表示
仕様
スペックシート
スペックシート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.
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:
- Gerald A.Rosenthal; Deborah Thomas. Radiochemical synthesis of dl-canaline and the colorimetric assay of canaline. Analytical Biochemistry. 1984, 140,(1), 246-249.
- 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.