| 词条 | Indolizidine |
| 释义 |
| ImageFile = Indolizidine.svg | ImageSize = 180px | IUPACName = Octahydroindolizine | OtherNames = δ-Coniceine; 1-Azabicyclo[4.3.0]nonane |Section1={{Chembox Identifiers | CASNo = 13618-93-4 | CASNo_Ref = {{cascite|correct|}} | PubChem = 26136 | ChemSpiderID = 24347 | SMILES = N12CCCC1CCCC2 | InChI = 1/C8H15N/c1-2-6-9-7-3-5-8(9)4-1/h8H,1-7H2 | InChIKey = HAJKHJOABGFIGP-UHFFFAOYAG | StdInChI = 1S/C8H15N/c1-2-6-9-7-3-5-8(9)4-1/h8H,1-7H2 | StdInChIKey = HAJKHJOABGFIGP-UHFFFAOYSA-N |Section2={{Chembox Properties | C=8 | H=15 | N=1 | Appearance = | Density = 0.8956 g/cm3 (20 °C)[1] | MeltingPt = | BoilingPtC = 159 to 160 | BoilingPt_ref = [2] | Solubility = |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} Indolizidine is a heterocyclic chemical compound that forms the central core of the indolizidine alkaloids such as swainsonine and castanospermine. See also
References1. ^{{Cite journal | title = 1-Azabicycles. IV. Catalytic synthesis of 1-azabicyclo[4.3.0]nonanes and 1-azabicyclo[5.3.0]decanes |author1=Skvortsov, I. M. |author2=Zadumina, E. A. |author3=Ponomarev, A. A. | journal = Khimiya Geterotsiklicheskikh Soedinenii | year = 1965 | volume = 6 | pages = 864–868}} {{heterocyclic-stub}}2. ^{{Cite journal | title = Conidine—Synthesis, Polymerization and Derivatives | author = Lavagnino, Edward R. | journal = Journal of the American Chemical Society | year = 1960 | volume = 82 | pages = 2609–2613 | doi = 10.1021/ja01495a054 | last2 = Chauvette | first2 = Robert R. | last3 = Cannon | first3 = William N. | last4 = Kornfeld | first4 = Edmund C. | issue = 10}} 1 : Indolizidines |
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