| Revision as of 12:14, 6 December 2011 editBeetstra (talk | contribs)Edit filter managers, Administrators172,031 edits Saving copy of the {{chembox}} taken from revid 450435957 of page Pyrrolizidine for the Chem/Drugbox validation project (updated: 'CASNo'). |
Latest revision as of 14:26, 11 June 2024 edit Marbletan (talk | contribs)Extended confirmed users5,350 editsNo edit summary |
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{{ambox | text = This page contains a copy of the infobox ({{tl|chembox}}) taken from revid of page ] with values updated to verified values.}} |
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{{chembox |
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{{chembox |
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| Verifiedfields = changed |
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| verifiedrevid = 401038328 |
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| verifiedrevid = 464377873 |
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|ImageFile= Pyrrolizidine.svg |
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| ImageFile= Pyrrolizidine.svg |
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|ImageSize=150px |
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| ImageSize=150px |
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|IUPACName=2,3,5,6,7,8-Hexahydro-1''H''-pyrrolizine |
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| PIN=Hexahydro-1''H''-pyrrolizine |
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|OtherNames=Hexahydropyrrolizine |
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| OtherNames=Hexahydropyrrolizine<br/> 1-Azabicyclooctane |
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|Section1={{Chembox Identifiers |
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|Section1={{Chembox Identifiers |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID = 12039 |
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| ChemSpiderID = 12039 |
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| InChI = 1/C7H13N/c1-3-7-4-2-6-8(7)5-1/h7H,1-6H2 |
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| InChI = 1/C7H13N/c1-3-7-4-2-6-8(7)5-1/h7H,1-6H2 |
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey = ADRDEXBBJTUCND-UHFFFAOYSA-N |
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| StdInChIKey = ADRDEXBBJTUCND-UHFFFAOYSA-N |
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| CASNo_Ref = {{cascite|correct|CAS}} |
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| CASNo = <!-- blanked - oldvalue: 643-20-9 --> |
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| CASNo=643-20-9 |
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| PubChem=12558 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| SMILES = N12CCCC1CCC2 |
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| UNII = U81KWZ2JKN |
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| PubChem=12558 |
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| SMILES = N12CCCC1CCC2 |
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}} |
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|Section2={{Chembox Properties |
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|Section2={{Chembox Properties |
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| Formula=C<sub>7</sub>H<sub>13</sub>N |
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| C = 7 | H = 13 | N = 1 |
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| MolarMass=111.18 g/mol |
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|Section3={{Chembox Hazards |
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|Section3={{Chembox Hazards |
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'''Pyrrolizidine''' is a ] ]. Formally, it is a ] derivative of ]. |
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Pyrrolizidine forms the central chemical structure of a variety of ]s known collectively as ]s.<ref> at ] {{Webarchive|url=https://web.archive.org/web/20160303182232/http://www.genome.jp/kegg-bin/get_htext?htext=br08003.keg&filedir=%2Ffiles&extend=A1&open=B10#B10 |date=2016-03-03 }}</ref> It is one of five classes of ]s. These are often synthesized from a carbohydrate.<ref>{{Cite journal|last=Lauritsen|first=Anne|last2=Madsen|first2=Robert|date=2006-07-19|title=Synthesis of naturally occurring iminosugars from D-fructose by the use of a zinc-mediated fragmentation reaction|journal=Organic & Biomolecular Chemistry|language=en|volume=4|issue=15|pages=2898–2905|doi=10.1039/B605818C|pmid=16855738|issn=1477-0539}}</ref> |
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==References== |
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{{reflist}} |
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{{heterocyclic-stub}} |
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] |