n-Propyl azide

n-Propyl azide
Names
	Preferred IUPAC name 1-Azidopropane
Identifiers
CAS Number	22293-25-0 ;
3D model (JSmol)	Interactive image;
ChemSpider	14073926 ;
PubChem CID	12405072;
UNII	TKS92J6VGG ;
CompTox Dashboard (EPA)	DTXSID60496682 ;
	InChI InChI=1S/C3H7N3/c1-2-3-5-6-4/h2-3H2,1H3 Key: TVPPZASKIXGUJQ-UHFFFAOYSA-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). verify (what is ?) 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

↑ 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. doi:10.1016/j.bmcl.2005.05.090. PMID 15993055.
↑ 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.