Heptene: Difference between revisions
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Updating {{chembox}} (no changed fields - added verified revid - updated 'DrugBank_Ref', 'UNII_Ref', 'ChEMBL_Ref', 'ChEBI_Ref', 'KEGG_Ref', 'ChEBI_Ref') per Chem/Drugbox validation (report [[Wikipedia_talk:WikiProject_Chemicals|error |
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{{Multiple issues|1= |
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{{more footnotes|date=June 2023}} |
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{{catimprove|date=June 2023}} |
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{{Distinguish|heptane|heptyne}} |
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{{Chembox |
{{Chembox |
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| Watchedfields = changed |
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| verifiedrevid = |
| verifiedrevid = 447805155 |
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| Name = 1-Heptene |
| Name = 1-Heptene |
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| ImageFile = |
| ImageFile = N-heptene structure.svg |
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| ImageSize = |
| ImageSize = |
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| PIN = Hept-1-ene |
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| OtherNames = |
| OtherNames = |
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|Section1={{Chembox Identifiers |
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| index1_label = 1-heptene |
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| index2_label = 2-heptene |
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| index3_label = 3-heptene |
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| index4_label = cis-2- |
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| index5_label = trans-2- |
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| CASNo2 = 592-77-8 |
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| CASNo3 = 592-78-9 |
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| EC_number2 = 209-768-3 |
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| EC_number3 = 209-769-9 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| UNII = O748KJ11V7 |
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| UNNumber = 2278 |
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| PubChem2 = 11611 |
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| PubChem3 = 11612 |
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| PubChem4 = 643836 |
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| PubChem5 = 639662 |
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| ChemSpiderID = 11121 |
| ChemSpiderID = 11121 |
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| InChI1_Ref = {{stdinchicite|correct|chemspider}} |
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| InChI1 = 1S/C7H14/c1-3-5-7-6-4-2/h3H,1,4-7H2,2H3 |
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| InChIKey1_Ref = {{stdinchicite|correct|chemspider}} |
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| InChIKey1 = ZGEGCLOFRBLKSE-UHFFFAOYSA-N |
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| SMILES1 = C=CCCCCC |
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| InChI3=1S/C7H14/c1-3-5-7-6-4-2/h5,7H,3-4,6H2,1-2H3 |
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| InChIKey3 = WZHKDGJSXCTSCK-UHFFFAOYSA-N |
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| SMILES3 = CCCC=CCC |
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| InChI4=1S/C7H14/c1-3-5-7-6-4-2/h3,5H,4,6-7H2,1-2H3/b5-3- |
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| InChIKey4 = OTTZHAVKAVGASB-HYXAFXHYSA-N |
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| SMILES4 = CCCC/C=C\C |
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| InChI5=1S/C7H14/c1-3-5-7-6-4-2/h3,5H,4,6-7H2,1-2H3/b5-3+ |
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| InChIKey5 = OTTZHAVKAVGASB-HWKANZROSA-N |
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| SMILES5 = CCCC/C=C/C |
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}} |
}} |
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|Section2={{Chembox Properties |
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| Properties_ref = <ref name=SA>[http://www.sigmaaldrich.com/catalog/product/aldrich/h3208?lang=en®ion=US 1-Heptene] at [[Sigma-Aldrich]]</ref> |
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| C=7 | H=14 |
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| Appearance = Colorless liquid |
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| Density = 0.697 g/mL |
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| MeltingPtC = -119 |
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| BoilingPtC = 94 |
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| Solubility = |
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|Section3={{Chembox Hazards |
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| Hazards_ref = <ref name=SA/> |
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| MainHazards = |
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| FlashPtC = -9 |
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| AutoignitionPtC = |
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| GHSPictograms = {{GHS02}}{{GHS08}}{{GHS09}} |
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| GHSSignalWord = Danger |
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| SPhrases = {{S16}} {{S26}} {{S36}} {{S62}} |
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| HPhrases = {{H-phrases|225|304|410}} |
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| PPhrases = {{P-phrases|210|233|240|241|242|243|273|280|301+310|303+361+353|331|370+378|391|403+235|405|501}} |
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The commercial product is a liquid that is a mixture of [[structural isomer|isomers]]. It is used as an additive in lubricants, as a [[catalyst]], and as a [[surfactant]]. This chemical is also known as heptylene. |
The commercial product is a liquid that is a mixture of [[structural isomer|isomers]]. It is used as an additive in lubricants, as a [[catalyst]], and as a [[surfactant]]. This chemical is also known as heptylene. |
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{{Gallery |mode=packed |align=center |
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}} |
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==References== |
==References== |
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{{reflist}} |
{{reflist}} |
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==Further reading== |
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* Carl Schaschke, 2014, ''[https://ebookcentral-proquest-com.ezproxy2.library.usyd.edu.au/lib/usyd/detail.action?docID=1591060 A Dictionary of Chemical Engineering]'', Oxford University Press. |
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* G. I. Nikishin, Yu. N. Ogibin & L. Kh. Rakhmatullina, 1975, ‘[https://link-springer-com.ezproxy2.library.usyd.edu.au/content/pdf/10.1007/BF00929657.pdf Peroxydisulfate-initiated reactions of 1-heptene with acetic and propionic acids]’, ''Bulletin of the Academy of Sciences of the USSR'', Division of chemical science, volume 23, pages1479–1483 |
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* Yu. D. Shenin, T. V. Kotenko & A. N. Egorenkova, Nystatin. IV. 1969, [https://link-springer-com.ezproxy2.library.usyd.edu.au/content/pdf/10.1007/BF00759817.pdf The heptaene component of samples of nystatin-nursimicin], ''Pharmaceutical Chemistry Journal volume '''3''''', pages 631–634 |
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* Nicholas E. Leadbeater, Cynthia B. McGowan, 2013, [https://www-taylorfrancis-com.ezproxy2.library.usyd.edu.au/books/9780429108303/chapters/10.1201/b14645-6 Experiment 2: Second-Order Elimination Reaction Preparation of Heptene from 2-Bromoheptane], ''Laboratory Experiments Using Microwave Heating'', chapter 3 |
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* E. S. Mortikov, M. I. Rozengart & B. A. Kazanskii, 1968, [https://link-springer-com.ezproxy2.library.usyd.edu.au/content/pdf/10.1007/BF00914644.pdf Dehydrocyclization of n-heptenes under conditions of a pulsed system and in the usual flow-type setup], ''Bulletin of the Academy of Sciences of the USSR, Division of chemical science'' volume 17, pages95–98(1968) |
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{{Alkenes}} |
{{Alkenes}} |
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{{Hydrides by group}} |
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[[Category:Alkenes]] |
[[Category:Alkenes]] |
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{{alkene-stub}} |
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{{hydrocarbon-stub}} |
{{hydrocarbon-stub}} |
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[[de:1-Hepten]] |
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[[es:Hepteno]] |
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[[it:Eptene]] |
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[[nl:1-hepteen]] |
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[[fi:Hepteeni]] |
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[[sv:Hepten]] |