![cover image](https://wikiwandv2-19431.kxcdn.com/_next/image?url=https://upload.wikimedia.org/wikipedia/commons/thumb/f/f2/N%252CO-Dimethylhydroxylamine_3D_ball.png/640px-N%252CO-Dimethylhydroxylamine_3D_ball.png&w=640&q=50)
N,O-Dimethylhydroxylamine
Chemical compound / From Wikipedia, the free encyclopedia
N,O-Dimethylhydroxylamine is a methylated hydroxylamine used to form so called 'Weinreb amides' for use in the Weinreb ketone synthesis.[2] It is commercially available as its hydrochloride salt.[1]
Quick Facts Names, Identifiers ...
![]() | |
![]() | |
Names | |
---|---|
Preferred IUPAC name
N-Methoxymethanamine | |
Other names
Methoxymethylamine; Methylmethoxyamine; HNMeOMe | |
Identifiers | |
3D model (JSmol) |
|
ChemSpider |
|
ECHA InfoCard | 100.012.960 ![]() |
PubChem CID |
|
UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
Properties | |
C2H7NO | |
Molar mass | 61.084 g·mol−1 |
Melting point | −97 °C (−143 °F; 176 K)[2] Hydrochloride salt: 112 to 115 °C (234 to 239 °F; 385 to 388 K) |
Boiling point | 43.2[2] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
Close