词条 | BPDA |
释义 |
| ImageFile = biphenyltetracarboxylic dianhydride.svg | ImageSize = 200px | IUPACName = 5,5’-Bi-2-benzofuran-1,1’,3,3’-tetrone | OtherNames = 3,3',4,4'-Biphenyltetracarboxylic dianhydride; 4,4'-Biphthalic dianhydride |Section1={{Chembox Identifiers | Abbreviations = BPDA | CASNo = 2420-87-3 | CASNo_Ref = {{cascite|correct|}} | PubChem = 75494 | ChemSpiderID = 68023 | SMILES = O=C4OC(=O)c3c4cc(c1ccc2C(=O)OC(=O)c2c1)cc3 | InChI = 1/C16H6O6/c17-13-9-3-1-7(5-11(9)15(19)21-13)8-2-4-10-12(6-8)16(20)22-14(10)18/h1-6H | InChIKey = WKDNYTOXBCRNPV-UHFFFAOYAA | StdInChI = 1S/C16H6O6/c17-13-9-3-1-7(5-11(9)15(19)21-13)8-2-4-10-12(6-8)16(20)22-14(10)18/h1-6H | StdInChIKey = WKDNYTOXBCRNPV-UHFFFAOYSA-N |Section2={{Chembox Properties | C=16 | H=6 | O=6 | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} BPDA or biphenyl-tetracarboxylic acid dianhydride is a monomer used in the production of some polyimides. Applications
Characteristics
AnalyticsThe chemical shifts in 1H and 13C NMR spectroscopy are given in the literature.[1] The melting point is 299 - 301 °C.[1] See also
References1. ^1 {{Cite journal|title=An Efficient Synthetic Method for 3,3',4,4'-Biphenyltetracarboxylic Anhydride|url=http://koreascience.or.kr/journal/view.jsp?kj=JCGMCS&py=2009&vnc=v30n9&sp=2161|journal=Bulletin of the Korean Chemical Society|volume=30|issue=9|pages=2161–2164|doi=10.5012/bkcs.2009.30.9.2161}} {{DEFAULTSORT:Bpda}} 3 : Monomers|Biphenyls|Carboxylic anhydrides |
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