| 词条 | 2-Methylthiophene |
| 释义 |
| ImageFile = Methylthiophen.svg | ImageSize = | ImageAlt = | IUPACName = | OtherNames = methylthiol |Section1={{Chembox Identifiers | CASNo = 554-14-3 | PubChem = 11126 | ChemSpiderID = 21168808 | EC_number = 209-063-0 | UNII = 7115JAP77A | StdInChI=1S/C5H6S/c1-5-3-2-4-6-5/h2-4H,1H3 | StdInChIKey = XQQBUAPQHNYYRS-UHFFFAOYSA-N | SMILES = CC1=CC=CS1 |Section2={{Chembox Properties | C=5|H=6|S=1 | MolarMass = | Appearance = colorless liquid | Density = 1.0168 g/cm3 | MeltingPtC = -63.4 | BoilingPtC = 112.6 | Solubility = }} |Section3={{Chembox Hazards | GHSPictograms = {{GHS02}}{{GHS07}} | GHSSignalWord = Danger | HPhrases = {{H-phrases|225|302|312|332}} | PPhrases = {{P-phrases|210|233|240|241|242|243|261|264|270|271|280|301+312|302+352|303+361+353|304+312|304+340|312|322|330|363|370+378|403+235|501}} | MainHazards = | FlashPt = | AutoignitionPt = }} }}2-Methylthiophene is an organosulfur compound with the formula CH3C4H3S. It is a colorless, flammable liquid. It can be produced by Wolff-Kishner reduction of thiophene-2-carboxaldehyde.[1] See also
References1. ^{{cite journal|title=Thiophene Series. V. Wolff-Kishner Reductions|authors=King, Wm. J.; Nord, F. F.|journal=Journal of Organic Chemistry|year=1949|volume=14|pages=638-42|doi=10.1021/jo01156a016}} {{DEFAULTSORT:Methylthiophene, 2-}} 1 : Thiophenes |
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