Kairine
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| Names
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Preferred IUPAC name
1-Methyl-1,2,3,4-tetrahydroquinolin-8-ol
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| Identifiers
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CAS Number
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- 5080-60-4
Y
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3D model (JSmol)
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| ChemSpider
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- 15544231
N
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| UNII
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- L2F6AD5R4V
Y
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InChI
InChI=1S/C10H13NO/c1-11-7-3-5-8-4-2-6-9(12)10(8)11/h2,4,6,12H,3,5,7H2,1H3 NKey: AXONCVPTTFHNOI-UHFFFAOYSA-N NInChI=1/C10H13NO/c1-11-7-3-5-8-4-2-6-9(12)10(8)11/h2,4,6,12H,3,5,7H2,1H3 Key: AXONCVPTTFHNOI-UHFFFAOYAE
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| Properties
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Chemical formula
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C10H13NO
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| Molar mass
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163.220 g·mol−1
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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N verify (what is Y N ?)
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| Infobox references
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Tracking categories (test):
Kairine is a derivative of tetrahydroquinoline which was first described by Wilhelm Fischer in 1883. Its name comes from the Greek kairos, meaning "the right time".[1] It is an antipyretic, formerly used against typhoid fever, but now largely obsolete due to severe side effects. Both kairine and its N-ethyl homolog show similar antipyretic activity.[2][3][4][5]
See also
References
- ↑ W.E.Flood (1963). The Origins of Chemical Names. Oldbourne Book Co Ltd. pp. 126.
- ↑ Fischer, Wilhelm (1883). "On Kairine and Kairoline". New Remedies 12 (2): 41. https://books.google.com/books?id=UVBHAQAAMAAJ&pg=PA41.
- ↑ Fruitnight, J. Henry (1886). "Kairine and Antipyrine". Medical Record 29 (23): 646–648. https://books.google.com/books?id=xNM-AQAAMAAJ&pg=PA646.
- ↑ Bockmuhl M, Dorzbach E. Antipyretics of the tetrahydroquinoline series. Med. u. Chem. (1942) 4: 179-212.
- ↑ Slater, Leo Barney (2009). War and Disease: Biomedical Research on Malaria in the Twentieth Century. Rutgers University Press. p. 26. ISBN 978-0-8135-4438-0.
 | Original source: https://en.wikipedia.org/wiki/Kairine. Read more |