N,O-Dimethylhydroxylamine
 | |
| Names | |
|---|---|
| IUPAC name
N-Methoxymethanamine | |
| Other names
Methoxymethylamine; Methylmethoxyamine; HNMeOMe | |
| Identifiers | |
1117-97-1  6638-79-5 (HCl)  | |
| ChemSpider | 13596 |
| |
| Jmol-3D images | Image |
| PubChem | 14232 |
| |
| Properties | |
| Molecular formula |
C2H7NO |
| Molar mass | 61.08 g·mol−1 |
| Melting point | 112 to 115 °C (234 to 239 °F; 385 to 388 K) (HCl) |
| Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
| verify (what is: /?) | |
| Infobox references | |
N,O-Dimethylhydroxylamine is used in amide coupling reactions to form Weinreb amides for use in the Weinreb ketone synthesis.[1]
It was identified as a microbial degradation product of the herbicide linuron formed in the presence of extracts of Bacillus sphaericus ATCC 12123 by characterization of its dinitrophenyl derivative.[2]
See Also
- Methoxyamine
- N-methylhydroxylamine
References
- ↑ 1.0 1.1 N,O-Dimethylhydroxylamine hydrochloride at Sigma-Aldrich
- ↑ G. Engelhardt, P. R. Wallnofer, R. Plapp (1972). "Identification of N, O-Dimethylhydroxylamine as a Microbial Degradation Product of the Herbicide, Linuron" (PDF). Applied Microbiology 23 (3): 664–666. PMC 380407. PMID 5021977.