Quinuclidine

Quinuclidine^[1]
Skeletal formula of quinuclidine	Ball-and-stick model of quinuclidine
Names
	Preferred IUPAC name 1-Azabicyclo[2.2.2]octane
	Other names Quinuclidine
Identifiers
CAS Number	100-76-5 ;
3D model (JSmol)	Interactive image;
Beilstein Reference	103111
ChEBI	CHEBI:38420 ;
ChEMBL	ChEMBL1209648 ;
ChemSpider	7246 ;
ECHA InfoCard	100.002.625
EC Number	202-887-1;
Gmelin Reference	26726
PubChem CID	7527;
UNII	XFX99FC5VI ;
CompTox Dashboard (EPA)	DTXSID2057607 ;
	InChI InChI=1S/C7H13N/c1-4-8-5-2-7(1)3-6-8/h7H,1-6H2 Key: SBYHFKPVCBCYGV-UHFFFAOYSA-N ; InChI=1/C7H13N/c1-4-8-5-2-7(1)3-6-8/h7H,1-6H2 Key: SBYHFKPVCBCYGV-UHFFFAOYAA;
	SMILES N12CCC(CC1)CC2;
Properties
Chemical formula	C7H13N
Molar mass	111.188 g·mol−1
Density	0.97 g/cm3
Melting point	157 to 160 °C (315 to 320 °F; 430 to 433 K)
Boiling point	149.5 °C (301.1 °F; 422.6 K) at 760 mmHg
Acidity (pKa)	11.0 (conjugate acid)
Hazards
	GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H301, H310, H315, H318
Precautionary statements	P262, P264, P264+P265, P270, P280, P301+P316, P302+P352, P305+P354+P338, P316, P317, P321, P330, P332+P317, P361+P364, P362+P364, P405, P501
Flash point	36.5 °C (97.7 °F; 309.6 K)
	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

Quinuclidine is an organic compound with the formula HC(C₂H₄)₃N. It is a bicyclic amine that can be viewed as a tied back version of triethylamine. It is a colorless solid. It is used as a reagent (base) and catalyst. It can be prepared by reduction of quinuclidone.

^ Quinuclidine Archived October 15, 2007, at the Wayback Machine at Sigma-Aldrich
^ ^a ^b Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 169. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4. The name quinuclidine is retained for general nomenclature only (see Table 2.6).
^ "Quinuclidine". pubchem.ncbi.nlm.nih.gov.

[1] Quinuclidine Archived October 15, 2007, at the Wayback Machine at Sigma-Aldrich

[iupac2013-2] Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 169. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4. The name quinuclidine is retained for general nomenclature only (see Table 2.6).

[3] "Quinuclidine". pubchem.ncbi.nlm.nih.gov.

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Quinuclidine

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