Wikipedia:WikiProject Chemicals/Chembox validation/VerifiedDataSandbox and 2,5-Dihydrofuran: Difference between pages
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Saving copy of the {{chembox}} taken from revid 442225392 of page 2,5-Dihydrofuran for the Chem/Drugbox validation project (updated: 'CASNo'). |
Undid revision 1079521778 by BazookaIce (talk) |
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{{short description|Chemical compound}} |
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{{ambox | text = This page contains a copy of the infobox ({{tl|chembox}}) taken from revid [{{fullurl:2,5-Dihydrofuran|oldid=442225392}} 442225392] of page [[2,5-Dihydrofuran]] with values updated to verified values.}} |
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{{chembox |
{{chembox |
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| Verifiedfields = changed |
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| Watchedfields = changed |
| Watchedfields = changed |
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| verifiedrevid = |
| verifiedrevid = 477211441 |
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| ImageFileL1=2,5-Dihydrofuran.svg |
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| ImageAltL1 = Skeletal formula of 2,5-dihydrofuran |
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| ImageSize=120px |
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| ImageFileR1 = 2,5-Dihydrofuran-3D-balls.png |
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| ImageSizeR1 = 130 |
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| ImageAltR1 = Ball-and-stick model of the 2,5-dihydrofuran molecule |
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| PIN=2,5-Dihydrofuran |
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| OtherNames= |
| OtherNames= |
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|Section1={{Chembox Identifiers |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID = 14813 |
| ChemSpiderID = 14813 |
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| InChI = 1/C4H6O/c1-2-4-5-3-1/h1-2H,3-4H2 |
| InChI = 1/C4H6O/c1-2-4-5-3-1/h1-2H,3-4H2 |
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey = ARGCQEVBJHPOGB-UHFFFAOYSA-N |
| StdInChIKey = ARGCQEVBJHPOGB-UHFFFAOYSA-N |
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| CASNo_Ref = {{cascite|correct|CAS}} |
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| CASNo = <!-- blanked - oldvalue: 1708-29-8 --> |
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| CASNo=1708-29-8 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| UNII = HD0TIE091T |
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|Section2={{Chembox Properties |
|Section2={{Chembox Properties |
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| C=4 | H=6 | O=1 |
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| H = 6 |
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| O = 1 |
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| BoilingPtC = 67.4 |
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| Solubility = |
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| Solubility = |
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|Section3={{Chembox Hazards |
|Section3={{Chembox Hazards |
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| MainHazards= |
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| FlashPt= |
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| AutoignitionPt = |
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| Autoignition= |
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'''2,5-Dihydrofuran''' is an [[organic compound]] classified as a monounsaturated derivative of [[furan]]. It is a colorless, volatile liquid. It can be produced from the acid-catalyzed rearrangement [[butadiene|1{{nbh}}butene 3,4{{nbh}}epoxide]].<ref>G. Wytze Meindersma, Matthias Maase and André B. Haan "Ionic Liquids" in Ullmann's Encyclopedia Of Industrial Chemistry 2007, Wiley-VCH, Weinheim. {{doi|10.1002/14356007.l14_l01}}</ref> |
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==References== |
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{{reflist}} |
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{{DEFAULTSORT:Dihydrofuran, 2, 5-}} |
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[[Category:Dihydrofurans]] |
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{{heterocyclic-stub}} |