5-nitroisoquinoline
Structural formula | ||||||||||||||||
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General | ||||||||||||||||
Surname | 5-nitroisoquinoline | |||||||||||||||
Molecular formula | C 9 H 6 N 2 O 2 | |||||||||||||||
Brief description |
yellow solid |
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properties | ||||||||||||||||
Molar mass | 174.16 g mol −1 | |||||||||||||||
Physical state |
firmly |
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Melting point |
106-109 ° 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 . |
5-Nitroisoquinoline is a heterocyclic chemical compound, which consists of an isoquinoline skeleton with a nitro group in the 5-position .
presentation
5-Nitroisoquinoline can be made by nitrating isoquinoline. The nitration takes place with high selectivity in the 5-position. This selectivity contrasts with the low selectivity of the nitration of the isomeric quinoline , from which a mixture of equal parts of 5- and 8-nitroquinoline is obtained.
Individual evidence
- ↑ a b Data sheet 5-nitroisoquinoline from AlfaAesar, accessed on July 18, 2010 ( PDF )(JavaScript required) .
- ↑ a b Data sheet 5-Nitroisoquinoline from Sigma-Aldrich , accessed on March 18, 2011 ( PDF ).
- ↑ JA Joules, K. Mills: Heterocyclic Chemistry , 5th Edition, pp. 177-199, Blackwell Publishing, Chichester, 2010, ISBN 978-1-4051-9365-8 .
- ↑ MW Austin, JH Ridd: The kinetics and mechanism of heteroaromatic nitration. Part I. Quinoline , in: J. Chem. Soc. 1963 : 4204-4210; doi : 10.1039 / JR9630004204 .