N,O-Dimethylhydroxylamine
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(Redirected from N,O-dimethylhydroxylamine)
| N,O-Dimethylhydroxylamine[1] | |
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N-Methoxymethanamine |
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Other names
Methoxymethylamine; Methylmethoxyamine |
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| Identifiers | |
| CAS number | 1117-97-1  , 6638-79-5 (HCl) |
| PubChem | 14232 |
| Jmol-3D images | Image 1 |
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| Properties | |
| Molecular formula | C2H7NO |
| Molar mass | 61.08 g mol−1 |
| Melting point |
112-115 °C (HCl) |
 (verify) (what is:  / ?)Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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| 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]
[edit] References
- ^ a b 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". Applied Microbiology 23 (3): 664–666. PMC 380407. PMID 5021977. http://aem.asm.org/cgi/reprint/23/3/664.pdf.
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