| Weight | 61.084 g/mol |
|---|---|
| Formula | C2H7NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
N,O-Dimethylhydroxylamine (1117-97-1)
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- The molecular structures of O-methylhydroxylamine, N-methylhydroxylamine, N,O-dimethylhydroxylamine and N,N,O-trimethylhydroxylamine in the gas phase, determined by electron diffraction (Journal of Molecular Structure, 1981)
- Identification of N, O-Dimethylhydroxylamine as a Microbial Degradation Product of the Herbicide, Linuron (Applied and Environmental Microbiology, 1972)
- Use of N,O-Dimethylhydroxylamine As an Anomeric Protecting Group in Carbohydrate Synthesis (Journal of Organic Chemistry, 2011)
- SYNTHESIS OF N,O-DIMETHYLHYDROXYLAMINE HYDROCHLORIDE (Organic Preparations and Procedures International, 1987)
- Dialkylaluminum N,O-dimethylhydroxylamine complex as a reagent to mask reactive carbonyl groups in situ from nucleophiles. (Organic Letters, 2010)
- REGIOSELECTIVE CC BOND FORMATION OF O-LINALYL-N,N-DIMETHYLHYDROXYLAMINE VIA CARBOPALLADATION (Chemistry Letters, 1979)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCNOC
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InChIKeyKRKPYFLIYNGWTE-UHFFFAOYSA-N
- Pubchem - N,O-Dimethylhydroxylamine
- Wikipedia - N-methoxymethylamine
N,O-Dimethylhydroxylamine is a methylated hydroxylamine used to form so called 'Weinreb amides' for use in the Weinreb ketone synthesis. It is commercially available as its hydrochloride salt.
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