Heptene: Difference between revisions

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{{more footnotes|date=June 2023}}

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{{Distinguish|heptane|heptyne}}

| Watchedfields = changed

| verifiedrevid = 447805155

| ImageFile = N-heptene structure.svg

| PIN = Hept-1-ene

|Section1={{Chembox Identifiers

| index1_label = 1-heptene

| index2_label = 2-heptene

| index3_label = 3-heptene

| index4_label = cis-2-

| index5_label = trans-2-

| CASNo1 = 592-76-7

| CASNo1_Ref = {{cascite|correct|CAS}}

| CASNo2 = 592-77-8

| CASNo3 = 592-78-9

| EC_number2 = 209-768-3

| EC_number3 = 209-769-9

| UNII_Ref = {{fdacite|correct|FDA}}

| UNII = O748KJ11V7

| UNNumber = 2278

| PubChem1 = 11610

| PubChem2 = 11611

| PubChem3 = 11612

| PubChem4 = 643836

| PubChem5 = 639662

| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}

| InChI1_Ref = {{stdinchicite|correct|chemspider}}

| InChI1 = 1S/C7H14/c1-3-5-7-6-4-2/h3H,1,4-7H2,2H3

| InChIKey1_Ref = {{stdinchicite|correct|chemspider}}

| InChIKey1 = ZGEGCLOFRBLKSE-UHFFFAOYSA-N

| SMILES1 = C=CCCCCC

| InChI3=1S/C7H14/c1-3-5-7-6-4-2/h5,7H,3-4,6H2,1-2H3

| InChIKey3 = WZHKDGJSXCTSCK-UHFFFAOYSA-N

| SMILES3 = CCCC=CCC

| InChI4=1S/C7H14/c1-3-5-7-6-4-2/h3,5H,4,6-7H2,1-2H3/b5-3-

| InChIKey4 = OTTZHAVKAVGASB-HYXAFXHYSA-N

| SMILES4 = CCCC/C=C\C

| InChI5=1S/C7H14/c1-3-5-7-6-4-2/h3,5H,4,6-7H2,1-2H3/b5-3+

| InChIKey5 = OTTZHAVKAVGASB-HWKANZROSA-N

| SMILES5 = CCCC/C=C/C

|Section2={{Chembox Properties

| Properties_ref = <ref name=SA>[http://www.sigmaaldrich.com/catalog/product/aldrich/h3208?lang=en&region=US 1-Heptene] at [[Sigma-Aldrich]]</ref>

| C=7 | H=14

| Appearance = Colorless liquid

| Density = 0.697 g/mL

| MeltingPtC = -119

| BoilingPtC = 94

| Solubility =

|Section3={{Chembox Hazards

| Hazards_ref = <ref name=SA/>

| MainHazards =

| FlashPtC = -9

| AutoignitionPtC =

| GHSPictograms = {{GHS02}}{{GHS08}}{{GHS09}}

| GHSSignalWord = Danger

| HPhrases = {{H-phrases|225|304|410}}

| PPhrases = {{P-phrases|210|233|240|241|242|243|273|280|301+310|303+361+353|331|370+378|391|403+235|405|501}}

'''Heptene''' is a higher [[olefin]], or [[alkene]] with the formula [[C7H14|C₇H₁₄]].

{{Gallery |mode=packed |align=center

|File:vapor_pressure_chart.svg|A log-lin vapor pressure chart of Heptene compared with various liquids

}}

==Further reading==

* 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.

* 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

* 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

* 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

* 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)

{{Hydrides by group}}

{{alkene-stub}}