| 词条 | 1-Fluoronaphthalene |
| 释义 |
| ImageFile = 1-fluoronaphthalene.svg | ImageSize = 180px | ImageAlt = | PIN = | OtherNames = α-fluoronaphthalene |Section1={{Chembox Identifiers | CASNo = 321-38-0 | CASNo_Ref = | EINECS = 206-287-0 | PubChem = 9450 | ChemSpiderID = 9078 | SMILES = C1=CC=C2C(=C1)C=CC=C2F | InChI = | InChIKey = | StdInChI = 1S/C10H7F/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H | StdInChIKey = CWLKTJOTWITYSI-UHFFFAOYSA-N | RTECS = | MeSHName = }} |Section2={{Chembox Properties | Formula = {{chem|C|10|H|7|F}} | MolarMass = | Appearance = Colorless liquid | Density = | MeltingPtC = −13 | BoilingPtC = 215 | Solubility = insoluble}} |Section3={{Chembox Hazards | MainHazards = | GHSPictograms = {{GHS07}} | GHSSignalWord = WARNING | FlashPtC = 65 | AutoignitionPt = }} }}1-Fluornaphthalene is an organofluorine chemical compound from the group of naphthalene derivatives and fluoroaromatics. Its chemical formula is {{chem|C|10|H|7|F}}.[1] Synthesis1-Fluoronaphthalene can be obtained by reacting naphthalene with Selectfluor.[2] Properties1-Fluornaphthalene is a colorless, combustible liquid, which is insoluble in water.[3] Applications1-Fluoronaphthalene was used for the tert-butyllithium-mediated synthesis of 6-substituted phenanthridines. It has also been used in the synthesis of LY248686, a potent inhibitor of serotonin and norepinephrine uptake. See also
References1. ^{{cite web|title=1-Fluoronaphthalene|url=http://www.sigmaaldrich.com/catalog/product/ALDRICH/196657?lang=en®ion=RU|website=Sigma Aldrich|publisher=sigmaaldrich.com|accessdate=13 June 2017}} {{DEFAULTSORT:Fluoronaphthalene, 1-}}2. ^{{cite book|last1=Atta-Ur-Rahman|title=Advances in Organic Synthesis: Modern Organofluorine Chemistry-Synthetic Aspects|date=2006|publisher=Bentham Science Publishers|isbn=1-60805-198-6|page=246}} 3. ^{{cite web|title=1-FLUORONAPHTHALENE|url=https://cameochemicals.noaa.gov/chemical/20415|website=CAMEO Chemicals|publisher=cameochemicals.noaa.gov|accessdate=13 June 2017}} 2 : Fluoroarenes|Naphthalenes |
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