Azepane
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Names | |||
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IUPAC name
Azepane | |||
Other names
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Identifiers | |||
3D model (JSmol) |
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ChEBI | |||
ChEMBL | |||
ChemSpider | |||
ECHA InfoCard | 100.003.524 | ||
PubChem CID |
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Properties | |||
C6H13N | |||
Molar mass | 99.18 g·mol−1 | ||
Density | 0.88 g/cm3[1] | ||
Boiling point | 138 °C (280 °F; 411 K)[1] (749 mmHg) | ||
Hazards | |||
Flash point | 18 °C (64 °F; 291 K) | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
Infobox references | |||
Azepane is a saturated heterocycle, containing one nitrogen atom in seven-membered ring.
Analogous to the well-known reaction of other amines,[2][3] azepane reacts with CO2 and in principle can be used for carbon capture.[4]
Azepane-containing drugs
- Amicibone
- Bacmecillinam (KW 1100)
- Beperidium
- Brazergoline
- Buzepide (Fenpipramide homolog).
- Cetiedil
- Gimantan
- Glidazamide
- Glisoxepide
- Glypinamide
- Hexacaine
- Mecillinam
- Molinate
- MR-16728 (cetiedil analogue)
- Nabazenil
- Pincainide
- Prozapine
- Setastine
- Tolazamide
- Pubchem 11142404
See also
References
- 1 2 "Hexamethyleneimine".
- ↑ Caplow, M. (1968). "Kinetics of Carbamate Formation and Breakdown". J. Am. Chem. Soc. 90 (24): 6795–6803. doi:10.1021/ja01026a041.
- ↑ Danckwerts, P. V. (1979). "The Reaction of CO2 with Ethanolamines". Chem. Eng. Sci. 34 (4): 443–446. doi:10.1016/0009-2509(79)85087-3.
- ↑ Sanz-Pérez, E. S.; Arencibia, A.; Sanz, R.; Calleja, G. (2016). "New developments on carbon dioxide capture using amine-impregnated silicas". Adsorption. 22 (4): 366–375. doi:10.1007/s10450-015-9740-2.
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