Aminoacetaldehyde diethylacetal
Aminoacetaldehyde diethylacetal is the organic compound with the formula (EtO)2CHCH2NH2. A colorless liquid, it is used as a surrogate for aminoacetaldehyde.[1][2]
2CHCH2NH2.png.webp) | |
| Names | |
|---|---|
| IUPAC name
2,2-Diethoxyethanamine | |
| Identifiers | |
3D model (JSmol) |
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| ChemSpider | |
| ECHA InfoCard | 100.010.401  |
| EC Number |
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PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C6H15NO2 | |
| Molar mass | 133.191 g·mol−1 |
| Appearance | colorless liquid |
| Density | 0.9152 g/cm3 |
| Melting point | −78 °C (−108 °F; 195 K) |
| Boiling point | 163 °C (325 °F; 436 K) |
| Hazards | |
| GHS pictograms |    |
| GHS Signal word | Danger |
| H226, H314, H315, H319, H335 | |
| P210, P233, P240, P241, P242, P243, P260, P261, P264, P271, P280, P301+330+331, P302+352, P303+361+353, P304+340, P305+351+338, P310, P312, P321, P332+313, P337+313, P362, P363, P370+378, P403+233 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
See also
References
- Fisher, Lawrence E.; Muchowski, Joseph M. (1990). "Synthesis of α-Aminoaldehydes and α-Aminoketone. A Review". Organic Preparations and Procedures International. 22 (4): 399–484. doi:10.1080/00304949009356309.
- Amato, Francesco; Marcaccini, Stefano (2005). "2,2-Diethoxy-1-Isocyanoethane". Organic Syntheses. 82: 18. doi:10.15227/orgsyn.082.0018.
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