| 词条 | N-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline |
| 释义 |
| Watchedfields = changed | verifiedrevid = 424811563 | Reference =[1] | Name = N-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline | ImageFile =EEDQ.png | ImageSize = | IUPACName =2-Ethoxy-2H-quinoline-1-carboxylic acid ethyl ester | OtherNames =Ethyl 1,2-dihydro-2-ethoxyquinoline-1-carboxylate |Section1={{Chembox Identifiers | Abbreviations = EEDQ | CASNo_Ref = {{cascite|correct|??}} | CASNo =16357-59-8 | PubChem =27833 | SMILES =CCOC1C=CC2=CC=CC=C2N1C(=O)OCC |Section2={{Chembox Properties | Formula =C14H17NO3 | MolarMass =247.29 g/mol | Appearance = | Density = | MeltingPtC = 62 to 67 | MeltingPt_notes = | BoilingPt = | Solubility = |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }}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] References1. ^2-Ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline at Sigma-Aldrich {{Dopamine antagonists}}{{DEFAULTSORT:Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline, N-}}{{heterocyclic-stub}}2. ^Neuroscience Letters 1992, 137(2), p.265 3. ^https://www.bachem.com/bachem/bachem/joust/index.cfm?idland=223 3 : Carbamates|Quinolines|Ethers |
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