| 词条 | 4-Vinylpyridine |
| 释义 |
| ImageFile = 4-vinylpyridine.svg | ImageSize = 130 | ImageAlt = | IUPACName = 4-ethenylpyridine | OtherNames = |Section1={{Chembox Identifiers | CASNo = 100-43-6 | PubChem = 7502 | ChemSpiderID = 7221 | EC_number = 202-852-0 | UNII = I56G67XM8D | Beilstein = 104506 | StdInChI=1S/C7H7N/c1-2-7-3-5-8-6-4-7/h2-6H,1H2 | StdInChIKey = KFDVPJUYSDEJTH-UHFFFAOYSA-N | SMILES = C=CC1=CC=NC=C1 |Section2={{Chembox Properties | C=7|H=7|N=1 | MolarMass = | Appearance = colorless liquid | Density = 0.988 g/cm3 | MeltingPt = | MeltingPt_notes = | BoilingPtC = 62-65 | BoilingPt_notes = 15 mmHg | Solubility = }} |Section3={{Chembox Hazards | GHSPictograms = {{GHS02}}{{GHS05}}{{GHS06}}{{GHS07}}{{GHS08}}{{GHS09}} | GHSSignalWord = Danger | HPhrases = {{H-phrases|226|301|314|315|317|319|330|334|411}} | PPhrases = {{P-phrases|210|233|240|241|242|243|260|261|264|270|271|272|273|280|284|285|301+310|301+330+331|302+352|303+361+353|304+340|304+341|305+351+338|310|320|321|330|332+313|333+313|337+313|342+311|362|363|370+378|391|403+233|403+235|405|501}} | MainHazards = | FlashPt = | AutoignitionPt = }} }}4-Vinylpyridine is an organic compound with the formula CH2CHC5H4N. It is a derivative of pyridine with a vinyl group in the 4-position. It is a colorless liquid, although impure samples are often brown. It is a monomeric precursor to specialty polymers. 4-Vinylpyridine is prepared by the condensation of 4-methylpyridine and formaldehyde.[1] See also
References1. ^{{cite encyclopedia|authors=Abe, Nobuyuki; Ichimura, Hisao; Kataoka, Toshiaki; Morishita, Sinji; Shimizu, Shinkichi; Shoji, Takayuki; Watanabe, Nanao. |encyclopedia=Ullmann's Encyclopedia of Industrial Chemistry|year=2007|publisher=Wiley-VCH|location=Weinheim|doi=10.1002/14356007.a22_399}} {{DEFAULTSORT:Vinylpyridine, 4-}} 3 : Pyridines|Monomers|Vinyl compounds |
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