词条 | 4-Vinylbenzyl chloride |
释义 |
| ImageFile = 4-VBC.png | ImageSize = 100 | ImageAlt = | PIN = 1-(Chloromethyl)-4-ethenylbenzene | OtherNames = 1-(Chloromethyl)-4-vinylbenzene α-Chloromethylstyrene |Section1={{Chembox Identifiers | CASNo = 1592-20-7 | EINECS = 250-005-9 | PubChem = 74126 | ChemSpiderID = 66739 | SMILES = C=Cc1ccc(cc1)CCl | StdInChI = 1S/C9H9Cl/c1-2-8-3-5-9(7-10)6-4-8/h2-6H,1,7H2 | StdInChIKey = ZRZHXNCATOYMJH-UHFFFAOYSA-N }} |Section2={{Chembox Properties | C=9|H=9|Cl=1 |MolarMass = 152.62 | Appearance = colorless liquid | Density = 1.083 | MeltingPtC = | BoilingPtC = 229 | Solubility = }} |Section3={{Chembox Hazards | MainHazards = alkylating agent | FlashPt = | AutoignitionPt = }} }} 4-Vinylbenzyl chloride is an organic compound with the formula ClCH2C6H4CH=CH2. It is a bifunctional molecule, featuring both vinyl and a benzylic chloride functional groups. It is a colorless liquid that is typically stored with a stabilizer to suppress polymerization. In combination with styrene, vinylbenzyl chloride is used as a comonomer in the production of chloromethylated polystyrene.[1] It is produced by the chlorination of vinyltoluene. Often vinyltoluene consists of a mixture of 3- and 4-vinyl isomers, in which case the vinylbenzyl chloride will also be produced as a mixture of isomers.[2] References1. ^Montheard, Jean Pierre; Jegat, Corinne; Camps, Marcel "Vinylbenzylchloride (chloromethylstyrene), polymers, and copolymers. Recent reactions and applications" Journal of Macromolecular Science, Reviews in Macromolecular Chemistry and Physics 1999, volume C39, pp. 135-174. {{DEFAULTSORT:Vinylbenzyl chloride, 4-}}2. ^{{citation | author=Denis H. James | author2=William M. Castor | contribution=Styrene | title=Ullmann's Encyclopedia of Industrial Chemistry | edition=7th | publisher=Wiley | year=2007 | page=1|doi=10.1002/14356007.a25_329.pub2| isbn=3527306730 }} 4 : Monomers|Vinyl compounds|Benzene derivatives|Organochlorides |
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