Weight | 103.121 g/mol |
---|---|
Formula | C4H9NO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 2 |
N-(2-Hydroxyethyl)acetamide (142-26-7)
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- Sigma-Aldrich - N-(2-Hydroxyethyl)acetamide41.60 - 117.00 USD
- Fisher Scientific - Search for N-(2-Hydroxyethyl)acetamide
- TCI - N-(2-Hydroxyethyl)acetamide18.00 - 125.00 USD
- Accelerated regression of carcinogen-induced preneoplastic hepatocyte foci by peroxisome proliferators, BR931, 4-chloro-6-(2, 3-xylidino)-2-pyrimidinylthio (N-B-hydroxyethyl)acetamide, and di-(2-ethylhexyl)phthalate (Carcinogenesis, 1984)
- Suppression of Choline-deficient Diet-induced Hepatocyte Membrane Lipid Peroxidation in Rats by the Peroxisome Proliferators 4-Chloro-6-(2,3-xylidino)-2-pyrimidinylthio(N--hydroxyethyl)acetamide and Di(2-ethylhexyl)phthalate (Cancer Research, 1986)
- Suppression of EGF binding in rat liver by the hypolipidemic peroxisome proliferators, 4-chloro-6-(2,3-xylidino)-2-pyrimidinylthio-(N--hydroxyethyl)acetamide and di(2-ethylhexyl)phthalate (Carcinogenesis, 1988)
- Structural studies on copper(II) complex containing (Z)-2-(2-Aminothiazol-4-yl)-N-(2-hydroxyethyl)-2-(hydroxyimino) acetamide, A model compound for a cephalosporin antibiotic cefdinir (Journal of Inorganic Biochemistry, 1997)
- Molecular dimensions and properties of N-[1-(2-hydroxyethyl)-2-nitro-1H-imidazol-1-yl]acetamide (SR2508) (Archives of Biochemistry and Biophysics, 1993)
- Utility of 2-cyano-N-(2-hydroxyethyl) acetamide in heterocyclic synthesis (European Journal of Chemistry, 2015)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(=O)NCCO
-
InChIKeyPVCJKHHOXFKFRP-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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