Misplaced Pages

N-Propyl azide: Difference between revisions

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Browse history interactively← Previous editContent deleted Content addedVisualWikitext
Revision as of 02:57, 27 March 2011 editRjwilmsiBot (talk | contribs)Bots, Pending changes reviewers1,602,950 editsm fixing page range dashes using AWB (7658)← Previous edit Latest revision as of 07:36, 19 July 2023 edit undoHeadbomb (talk | contribs)Edit filter managers, Autopatrolled, Extended confirmed users, Page movers, File movers, New page reviewers, Pending changes reviewers, Rollbackers, Template editors454,506 edits ce 
(18 intermediate revisions by 16 users not shown)
Line 1: Line 1:
{{DISPLAYTITLE:''n''-Propyl azide}} {{DISPLAYTITLE:''n''-Propyl azide}}
{{chembox {{chembox
| Verifiedfields = changed
| Watchedfields = changed | Watchedfields = changed
| verifiedrevid = 411102772 | verifiedrevid = 420919817
| Name = ''n''-Propyl azide | Name = ''n''-Propyl azide
| ImageFile = Propyl azide.svg | ImageFile = Propyl azide.svg
| ImageAlt = Skeletal formula of propyl azide
| ImageSize =
| ImageFile1 = Propyl-azide-3D-balls.png
⚫ | IUPACName = 1-Azidopropane
| ImageSize1 = 190
| ImageAlt1 = Ball-and-stick model of the propyl azide molecule
⚫ | PIN = 1-Azidopropane
| OtherNames = | OtherNames =
| Section1 = {{Chembox Identifiers |Section1={{Chembox Identifiers
| CASNo =22293-25-0 | CASNo =22293-25-0
| CASNo_Ref = {{cascite|correct|CAS}} | CASNo_Ref = {{cascite|correct|CAS}}
| PubChem = | PubChem = 12405072
| SMILES ===NCCC | SMILES ===NCCC
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 14073926
| InChI = 1/C3H7N3/c1-2-3-5-6-4/h2-3H2,1H3
| InChIKey = TVPPZASKIXGUJQ-UHFFFAOYAK
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 1S/C3H7N3/c1-2-3-5-6-4/h2-3H2,1H3
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = TVPPZASKIXGUJQ-UHFFFAOYSA-N

}} }}
| Section2 = {{Chembox Properties |Section2={{Chembox Properties
| C=3 | H=7 | N=3 | C=3 | H=7 | N=3
| Appearance = | Appearance =
Line 23: Line 36:
| SolubleOther = | SolubleOther =
}} }}
| Section3 = {{Chembox Explosive |Section3={{Chembox Explosive
| ShockSens = | ShockSens =
| FrictionSens = | FrictionSens =
| ExplosiveV = | DetonationV =
| REFactor = }} | REFactor = }}
| Section4 = {{Chembox Hazards |Section4={{Chembox Hazards
| MainHazards = Harmful, Explosive | MainHazards = Harmful, Explosive
| FlashPt = | FlashPt =
| Autoignition = }} | AutoignitionPt = }}
| Section8 = {{Chembox Related |Section8={{Chembox Related
| OtherAnions = | OtherAnions =
| OtherCations = | OtherCations =
| OtherFunctn = | OtherFunction =
| Function = | OtherFunction_label =
| OtherCpds = ], ], ] }} | OtherCompounds = ], ], ] }}
}} }}


'''''n''-Propyl azide''' is an ] with the formula CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>N<sub>3</sub>. A white solid, it is a simple ].
'''''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> <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 = 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> ''n''-Propyl azide has been used in the laboratory synthesis of pharmaceutical drug candidates.<ref>{{Cite journal | author = Helmut Haning| title = Comparison of different heterocyclic scaffolds as substrate analog PDE5 inhibitors | journal = ] | year = 2005 | volume = 15 | issue = 17 | pages = 3900–3907 | doi=10.1016/j.bmcl.2005.05.090| pmid = 15993055 |display-authors=etal}}</ref><ref>{{cite journal | author = Michael H. Parker| 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 | doi=10.1016/s0968-0896(02)00251-1|display-authors=etal | pmid=12213471}}</ref>


==References== ==References==
Line 48: Line 62:


==Further reading== ==Further reading==
* {{cite journal | author = Edward J. Kaufmann, Richard C. Thompson | title = Reduction of organic azides by chromium(II) in aqueous solution | journal = ] | year = 1977 | volume = 99 | issue = 6 | pages = 1824–1830 | doi = 10.1021/ja00448a025}} * {{cite journal | author = Edward J. Kaufmann, Richard C. Thompson | title = Reduction of organic azides by chromium(II) in aqueous solution | journal = ] | year = 1977 | volume = 99 | issue = 6 | pages = 1824–1830 | doi = 10.1021/ja00448a025}}


{{DEFAULTSORT:Propyl azide, n-}} {{DEFAULTSORT:Propyl azide, n-}}
] ]
]




Latest revision as of 07:36, 19 July 2023

n-Propyl azide
Skeletal formula of propyl azide
Ball-and-stick model of the propyl azide molecule
Names
Preferred IUPAC name 1-Azidopropane
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
PubChem CID
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C3H7N3/c1-2-3-5-6-4/h2-3H2,1H3Key: TVPPZASKIXGUJQ-UHFFFAOYSA-N
  • InChI=1/C3H7N3/c1-2-3-5-6-4/h2-3H2,1H3Key: TVPPZASKIXGUJQ-UHFFFAOYAK
SMILES
  • ==NCCC
Properties
Chemical formula C3H7N3
Molar mass 85.110 g·mol
Hazards
Occupational safety and health (OHS/OSH):
Main hazards Harmful, Explosive
Related compounds
Related compounds Hydrazoic acid, Chlorine azide, Ethyl azide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒N verify (what is  ?) Infobox references
Chemical compound

n-Propyl azide is an organic compound with the formula CH3CH2CH2N3. A white solid, it is a simple organic azide.

n-Propyl azide has been used in the laboratory synthesis of pharmaceutical drug candidates.

References

  1. Stefan Bräse (Editor), Klaus Banert (Co-Editor); Organic Azides: Syntheses and Applications; 2010 John Wiley and Sons; ISBN 978-0-470-51998-1
  2. Helmut Haning; et al. (2005). "Comparison of different heterocyclic scaffolds as substrate analog PDE5 inhibitors". Bioorganic & Medicinal Chemistry Letters. 15 (17): 3900–3907. doi:10.1016/j.bmcl.2005.05.090. PMID 15993055.
  3. 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. doi:10.1016/s0968-0896(02)00251-1. PMID 12213471.

Further reading


Stub icon

This article about an organic compound is a stub. You can help Misplaced Pages by expanding it.

Categories: