Weight | 102.093 g/mol |
---|---|
Formula | C3H6N2O2 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
3-Amino-2-oxazolidinone (80-65-9)
3-amino-2-oxazolidone
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- Depletion of proteinbound furazolidone metabolites containing the 3amino2oxazolidinone sidechain from liver, kidney and muscle tissues from pigs (Food Additives and Contaminants Part A-chemistry Analysis Control Exposure & Risk Assessment, 1992)
- Determination of the furazolidone metabolite, 3-amino-2-oxazolidinone, in porcine tissues using liquid chromatography-thermospray mass spectrometry and the occurrence of residues in pigs produced in Northern Ireland (Journal of Chromatography B: Biomedical Sciences and Applications, 1997)
- Highly Stereoselective Intermolecular Radical Addition to Aldehyde Hydrazones from a Chiral 3-Amino-2-oxazolidinone (Journal of the American Chemical Society, 2000)
- Production and characterisation of polyclonal antibodies to a derivative of 3-amino-2-oxazolidinone, a metabolite of the nitrofuran furazolidone (Analytica Chimica Acta, 2004)
- Monoclonal antibody-based ELISA for the quantification of nitrofuran metabolite 3-amino-2-oxazolidinone in tissues using a simplified sample preparation (Analytica Chimica Acta, 2005)
- 6-O-Benzyl- and 6-O-Silyl-N-acetyl-2-amino-2-N,3-O-carbonyl-2-deoxyglucosides: Effective Glycosyl Acceptors in the Glucosamine 4-OH Series. Effect of Anomeric Stereochemistry on the Removal of the Oxazolidinone Group (Journal of Organic Chemistry, 2005)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3-amino-2-oxazolidone
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SMILESC1COC(=O)N1N
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InChIKeyKYCJNIUHWNJNCT-UHFFFAOYSA-N
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