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| '''''n''-Propyl azide''' is a covalent molecule related to ] and other ]s.<ref>Stefan Bräse (Editor), Klaus Banert (Co-Editor); ''Organic Azides: Syntheses and Applications''; 2010 ]; ISBN 978-0-470-51998-1</ref> | '''''n''-Propyl azide''' is a covalent molecule related to ] and other ]s.<ref>Stefan Bräse (Editor), Klaus Banert (Co-Editor); ''Organic Azides: Syntheses and Applications''; 2010 ]; ISBN 978-0-470-51998-1</ref> | ||
| ''n''-Propyl azide has been used in the laboratory synthesis of pharmaceutical drug candidates.<ref>{{Cite journal | author = Helmut Haning ''et al'' | title = Comparison of different heterocyclic scaffolds as substrate analog PDE5 inhibitors | journal = ] | year = 2005 | volume = 15 | issue = 17 | pages = |
''n''-Propyl azide has been used in the laboratory synthesis of pharmaceutical drug candidates.<ref>{{Cite journal | author = Helmut Haning ''et al'' | title = Comparison of different heterocyclic scaffolds as substrate analog PDE5 inhibitors | journal = ] | year = 2005 | volume = 15 | issue = 17 | pages = 3900–3907}}</ref><ref>{{cite journal | author = Michael H. Parker ''et al'' | title = Synthesis of (-)-5,8-Dihydroxy-3R-methyl-2R-(dipropylamino)-1,2,3,4-tetrahydronaphthalene: An Inhibitor of β-Amyloid<sub>1-42</sub> Aggregation | journal = ] | year = 2002 | volume = 10 | issue = 11 | pages = 3565–3569}}</ref> | ||
| ==References== | ==References== | ||
Revision as of 02:57, 27 March 2011
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| Names | |
|---|---|
| IUPAC name 1-Azidopropane | |
| Identifiers | |
| CAS Number | |
| 3D model (JSmol) | |
| CompTox Dashboard (EPA) | |
SMILES
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| Properties | |
| Chemical formula | C3H7N3 |
| Molar mass | 85.110 g·mol |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
| Main hazards | Harmful, Explosive |
| Related compounds | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).
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Infobox references
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n-Propyl azide is a covalent molecule related to hydrazoic acid and other alkyl azides.
n-Propyl azide has been used in the laboratory synthesis of pharmaceutical drug candidates.
References
- Stefan Bräse (Editor), Klaus Banert (Co-Editor); Organic Azides: Syntheses and Applications; 2010 John Wiley and Sons; ISBN 978-0-470-51998-1
- Helmut Haning; et al. (2005). "Comparison of different heterocyclic scaffolds as substrate analog PDE5 inhibitors". Bioorganic & Medicinal Chemistry Letters. 15 (17): 3900–3907.
{{cite journal}}: Explicit use of et al. in:|author=(help) - Michael H. Parker; et al. (2002). "Synthesis of (-)-5,8-Dihydroxy-3R-methyl-2R-(dipropylamino)-1,2,3,4-tetrahydronaphthalene: An Inhibitor of β-Amyloid1-42 Aggregation". Bioorganic & Medicinal Chemistry. 10 (11): 3565–3569.
{{cite journal}}: Explicit use of et al. in:|author=(help)
Further reading
- Edward J. Kaufmann, Richard C. Thompson (1977). "Reduction of organic azides by chromium(II) in aqueous solution". JACS. 99 (6): 1824–1830. doi:10.1021/ja00448a025.
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