Indolizidine
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| General | |||||||||||||||||||
| Surname | Indolizidine | ||||||||||||||||||
| other names |
Octahydroindolizine |
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| Molecular formula | C 8 H 15 N | ||||||||||||||||||
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| properties | |||||||||||||||||||
| Molar mass | 125.2114 g mol −1 | ||||||||||||||||||
| Physical state |
firmly |
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| density |
0.907 g cm −3 |
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| Melting point |
75 ° C |
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| solubility |
easily soluble in ethanol and diethyl ether |
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| Refractive index |
1.4748 (20 ° C) |
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| safety instructions | |||||||||||||||||||
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| As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . Refractive index: Na-D line , 20 ° C | |||||||||||||||||||
Indolizidine is a chemical compound from the group of heterocyclic compounds that forms the central core of indolizidine alkaloids such as swainsonine and castanospermine . It is the perhydro derivative of indolizine .
Individual evidence
- ↑ a b c d David R. Lide: CRC Handbook of Chemistry and Physics A Ready-reference Book of Chemical and Physical Data . CRC Press, 1995, ISBN 978-0-8493-0595-5 , pp. 438 ( limited preview in Google Book search).
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
- ↑ JP Felix D'Mello: Handbook of Plant and Fungal Toxicants . CRC Press, 2020, ISBN 978-1-00-008339-2 ( limited preview in Google Book Search).
Web links
Commons : Indolizidine - Collection of pictures, videos and audio files