4,5-dinitroveratrol
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| General | |||||||||||||
| Surname | 4,5-dinitroveratrol | ||||||||||||
| other names |
1,2-dimethoxy-4,5-dinitrobenzene |
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| Molecular formula | C 8 H 8 N 2 O 6 | ||||||||||||
| Brief description |
yellow crystals |
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| properties | |||||||||||||
| Molar mass | 228.16 g · mol -1 | ||||||||||||
| Physical state |
firmly |
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| Melting point |
130-132 ° 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 . | |||||||||||||
4,5-Dinitroveratrol is a chemical compound that belongs to both the dimethoxybenzenes and the nitroaromatics .
presentation
One synthesis is based on veratrol , which is nitrated with nitric acid and sulfuric acid to 4,5-dinitroveratrol.
Complete methylation of 4,5-dinitrocatechol also leads to 4,5-dinitroveratrol.
Individual evidence
- ^ A b c J. Buckingham: "Dictionary of organic compounds", Volume 9, p. 2768 ( limited preview in the 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.
- ↑ Reinhardt B. Baudy, Lynne P. Greenblatt, Ivo L. Jirkovsky, Mary Conklin, Ralph J. Russo, Donna R. Bramlett, Tracy A. Emrey, Joanne T. Simmonds, Dianne M. Kowal: "Potent quinoxaline-spaced phosphono -a-amino acids of the AP-6 type as competitive NMDA antagonists: Synthesis and biological evaluation ", in: J. Med. Chem. , 1993 , 36 (3), pp. 331-342; doi : 10.1021 / jm00055a004 .