N-Propyl azide

n-Propyl azide

Names
Preferred IUPAC name 1-Azidopropane
Identifiers
CAS Number	22293-25-0  Y
3D model (JSmol)	Interactive image
ChemSpider	14073926  N
PubChem CID	12405072
CompTox Dashboard (EPA)	DTXSID60496682
InChI InChI=1S/C3H7N3/c1-2-3-5-6-4/h2-3H2,1H3 N Key: TVPPZASKIXGUJQ-UHFFFAOYSA-N N InChI=1/C3H7N3/c1-2-3-5-6-4/h2-3H2,1H3 Key: TVPPZASKIXGUJQ-UHFFFAOYAK
SMILES [N-]=[N+]=NCCC
Properties
Chemical formula	C3H7N3
Molar mass	85.110 g·mol−1
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 [77 °F], 100 kPa). N  verify  (what is  YN ?) Infobox references

n-Propyl azide is an organic compound with the formula CH₃CH₂CH₂N₃. A white solid, it is a simple organic azide. ^[1]

n-Propyl azide has been used in the laboratory synthesis of pharmaceutical drug candidates. ^{[2] [3]}

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-Amyloid_1-42 Aggregation". Bioorganic & Medicinal Chemistry . 10 (11): 3565–3569. doi:10.1016/s0968-0896(02)00251-1. PMID   12213471.

Further reading

• Edward J. Kaufmann, Richard C. Thompson (1977). "Reduction of organic azides by chromium(II) in aqueous solution". Journal of the American Chemical Society . 99 (6): 1824–1830. doi:10.1021/ja00448a025.