Butyrophenone
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| General | ||||||||||||||||
| Surname | Butyrophenone | |||||||||||||||
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| Molecular formula | C 10 H 12 O | |||||||||||||||
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| properties | ||||||||||||||||
| Molar mass | 148.20 g mol −1 | |||||||||||||||
| Physical state |
liquid |
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| density |
1.021 g cm −3 (25 ° C) |
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| Melting point |
11-13 ° C |
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| boiling point |
228-230 ° C |
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| Refractive index |
1.520 (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 | ||||||||||||||||
Butyrophenone is an aromatic organic-chemical compound and belongs to the ketones . It is the starting compound of the butyrophenones .
It can be made by Friedel-Crafts acylation of benzene with butyryl chloride . The Lewis acid aluminum chloride (AlCl 3 ) acts as a catalyst .
Some of its derivatives are commonly used neuroleptics , such as haloperidol and melperone . Their effect is based on the inhibition of (D 2 ) dopamine receptors .
Individual evidence
- ↑ a b c d e f data sheet butyrophenone from Sigma-Aldrich , accessed on September 6, 2016 ( PDF ).
- ↑ Axel M. Gressner, Torsten Arndt (Ed.): Lexicon of the Medical Laboratory Diagnostics . 2., revised. and exp. Edition. Springer, Berlin, Heidelberg 2013, ISBN 978-3-642-12921-6 , entry on Butyrophenone , doi : 10.1007 / 978-3-642-12921-6 .
- ↑ Thomas Efferth: Molecular pharmacology and toxicology: biological bases of drugs and poisons . Springer, Berlin, Heidelberg 2006, ISBN 3-540-21223-X , pp. 64 .