8-Aminoquinoline

8-Aminoquinoline
Names
	Preferred IUPAC name Quinolin-8-amine
Identifiers
CAS Number	578-66-5 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL99932 ;
ChemSpider	10881 ;
ECHA InfoCard	100.008.572
PubChem CID	11359;
UNII	U34EAV21TG ;
CompTox Dashboard (EPA)	DTXSID4060369 ;
	InChI InChI=1S/C9H8N2/c10-8-5-1-3-7-4-2-6-11-9(7)8/h1-6H,10H2 Key: WREVVZMUNPAPOV-UHFFFAOYSA-N ;
	SMILES Nc1cccc2cccnc12;
Properties
Chemical formula	C9H8N2
Molar mass	144.177 g·mol−1
Appearance	pale yellow solid
Density	1.337 g/cm3
Melting point	65 °C (149 °F; 338 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

8-Aminoquinoline is the 8-amino derivative of quinoline. Often abbreviated AQ, it is a pale yellow solid. It is structurally analogous to 8-hydroxyquinoline.^[2]

^ Van Meervelt L, Goethals M, Leroux N, Zeegers-Huyskens T (1997). "X-ray and vibrational studies of 8-aminoquinoline. Evidence for a three-center hydrogen bond". Journal of Physical Organic Chemistry. 10 (9): 680–686. doi:10.1002/(SICI)1099-1395(199709)10:9<680::AID-POC902>3.0.CO;2-Y.
^ Rej S, Ano Y, Chatani N (2020). "Bidentate Directing Groups: An Efficient Tool in C–H Bond Functionalization Chemistry for the Expedient Construction of C–C Bonds". Chemical Reviews. 120 (3): 1788–1887. doi:10.1021/acs.chemrev.9b00495. PMID 31904219. S2CID 209895281.

[1] Van Meervelt L, Goethals M, Leroux N, Zeegers-Huyskens T (1997). "X-ray and vibrational studies of 8-aminoquinoline. Evidence for a three-center hydrogen bond". Journal of Physical Organic Chemistry. 10 (9): 680–686. doi:10.1002/(SICI)1099-1395(199709)10:9<680::AID-POC902>3.0.CO;2-Y.

[2] Rej S, Ano Y, Chatani N (2020). "Bidentate Directing Groups: An Efficient Tool in C–H Bond Functionalization Chemistry for the Expedient Construction of C–C Bonds". Chemical Reviews. 120 (3): 1788–1887. doi:10.1021/acs.chemrev.9b00495. PMID 31904219. S2CID 209895281.

[1]

[2]