Cyclononanone
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| General | ||||||||||||||||
| Surname | Cyclononanone | |||||||||||||||
| Molecular formula | C 9 H 16 O | |||||||||||||||
| Brief description |
colorless solid |
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| properties | ||||||||||||||||
| Molar mass | 140.22 g mol −1 | |||||||||||||||
| Physical state |
firmly |
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| density |
0.959 g cm −3 (25 ° C) |
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| Melting point |
24-26 ° C |
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| boiling point |
95–97 ° C (24 hPa) |
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| solubility |
soluble in ethanol |
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| Refractive index |
1.477 (20 ° C) |
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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 | ||||||||||||||||
Cyclononanone is a chemical compound from the group of cycloalkanones .
Extraction and presentation
Cyclononanone can be obtained by reacting 1- (aminomethyl) -cyclooctanol with nitrous acid . Other syntheses are also known.
properties
Cyclononanone is a colorless solid.
Individual evidence
- ↑ a b c d e f g h i data sheet Cyclononanone, 95% from Sigma-Aldrich , accessed on May 3, 2015 ( PDF ).
- ↑ William M. Haynes: CRC Handbook of Chemistry and Physics, 95th Edition: . CRC Press, 2014, ISBN 978-1-4822-0868-9 , pp. 137 ( limited preview in Google Book search).
- ^ Calvin L. Stevens, Carl R. Johnson, Don C. de Jongh, Norman L. Allinger, Michael P. Cava: Gnichtel, Horst: Organische Chemie. [Hauptbd.] . Walter de Gruyter, 1980, ISBN 978-3-11-082970-9 , pp. 1241 ( limited preview in Google Book search).
- ↑ WJ Mijs, CRHI de Jonge: Organic Synthesis by oxidation with Metal Compounds: . Springer Science & Business Media, 2013, ISBN 978-1-4613-2109-5 , pp. 95 ( limited preview in Google Book search).