Formaldoxime
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| Names | |
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| Preferred IUPAC name
N-Hydroxymethanimine | |
| Identifiers | |
3D model (JSmol)
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| ECHA InfoCard | Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value).Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value). |
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| E number | Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| H2C=N−OH | |
| Molar mass | 45.041 g·mol−1 |
| Appearance | colorless liquid |
| Melting point | 2.5 °C (36.5 °F; 275.6 K) |
| Boiling point | 84 °C (183 °F; 357 K) |
| Hazards | |
| GHS labelling: | |
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Related compounds
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Formaldoxime is the organic compound with the formula H2C=N−OH. It is the oxime of formaldehyde. A colorless liquid, the pure compound tends to polymerize into a cyclic trimer. Aqueous solutions are stable as is the formaldoxime hydrochloride ([H2C=N(−H)(−OH)]+Cl−). It is a reagent in organic synthesis for the conversion of aryl diazonium salts to aryl aldehydes.[1]
It is generated by combining hydroxylamine and formaldehyde.[2]
Synonyms
[edit | edit source]Source:[3]
- Formoxime
- Nitrone
- Formaldehyde oxime
- formaldoxim
- methylenenitrone
References
[edit | edit source]- ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
- ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
- ^ https://pubchem.ncbi.nlm.nih.gov/compound/Formaldoxime#section=Depositor-Supplied-Synonyms&fullscreen=true
