N-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline

N-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline^[1]
Names
	Preferred IUPAC name Ethyl 2-ethoxyquinoline-1(2H)-carboxylate
	Other names Ethyl 1,2-dihydro-2-ethoxyquinoline-1-carboxylate
Identifiers
CAS Number	16357-59-8 ;
3D model (JSmol)	Interactive image;
Abbreviations	EEDQ
ECHA InfoCard	100.036.728
PubChem CID	27833;
UNII	60O971AN19 ;
CompTox Dashboard (EPA)	DTXSID50871969 ;
	SMILES CCOC1C=CC2=CC=CC=C2N1C(=O)OCC;
Properties
Chemical formula	C14H17NO3
Molar mass	247.29 g/mol
Melting point	62 to 67 °C (144 to 153 °F; 335 to 340 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

N-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ) is an irreversible dopamine-receptor antagonist.^[2]

EEDQ is also a highly specific reagent for carboxyl groups. It enables the coupling of acylamino acids with amino acid esters in high yield and without racemization.^[3]

It is also an irreversible dopamine transporter (DAT) blocker in vitro, though it is ineffective in vivo.^[4]

References

^ 2-Ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline at Sigma-Aldrich
^ Neuroscience Letters 1992, 137(2), p.265
^ https://www.bachem.com/
^ Tarazi FI, Kula NS, Zhang K, Baldessarini RJ (August 2000). "Alkylation of rat dopamine transporters and blockade of dopamine uptake by EEDQ". Neuropharmacology. 39 (11): 2133–8. doi:10.1016/s0028-3908(00)00047-2. PMID 10963756.

This article about a heterocyclic compound is a stub. You can help Wikipedia by expanding it.

[1] 2-Ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline at Sigma-Aldrich

[2] Neuroscience Letters 1992, 137(2), p.265

[3] https://www.bachem.com/

[pmid10963756-4] Tarazi FI, Kula NS, Zhang K, Baldessarini RJ (August 2000). "Alkylation of rat dopamine transporters and blockade of dopamine uptake by EEDQ". Neuropharmacology. 39 (11): 2133–8. doi:10.1016/s0028-3908(00)00047-2. PMID 10963756.

[1]

[2]

[3]

[4]