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]
Names | |
---|---|
IUPAC name
2,2-Diethoxyethanamine | |
Identifiers | |
3D model (JSmol) |
|
ChemSpider | |
ECHA InfoCard | 100.010.401 |
EC Number |
|
PubChem CID |
|
UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
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.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.