| Revision as of 15:40, 1 July 2011 editAmirobot (talk | contribs)56,602 editsm r2.7.1) (robot Adding: nl:Oxepaan← Previous edit |
Latest revision as of 15:55, 18 August 2022 edit undoFswitzer4 (talk | contribs)Extended confirmed users10,572 editsm Added UNII |
| (16 intermediate revisions by 15 users not shown) |
| Line 1: |
Line 1: |
|
{{chembox |
|
{{chembox |
|
|
| Verifiedfields = changed |
| ⚫ |
| verifiedrevid = 413360343 |
|
|
|
| Watchedfields = changed |
| ⚫ |
|ImageFile=Oxepan.png |
|
|
⚫ |
| verifiedrevid = 437245898 |
| ⚫ |
|ImageSize=100 |
|
|
⚫ |
| ImageFile = Oxepane.svg |
|
|IUPACName=oxepane |
|
|
⚫ |
| ImageSize = 100px |
|
|OtherNames= |
|
|
|
| PIN = Oxepane |
| ⚫ |
|Section1={{Chembox Identifiers |
|
|
|
| OtherNames = Hexamethylene oxide |
| ⚫ |
| CASNo=592-90-5 |
|
|
|
|
| ⚫ |
| PubChem=11618 |
|
|
⚫ |
| Section1 = {{Chembox Identifiers |
| ⚫ |
| SMILES=C1CCCOCC1 |
|
|
|
| CASNo_Ref = {{cascite|correct|??}} |
| ⚫ |
}} |
|
|
⚫ |
| CASNo = 592-90-5 |
| ⚫ |
|Section2={{Chembox Properties |
|
|
|
| UNII_Ref = {{fdacite|correct|FDA}} |
| ⚫ |
| Formula=C<sub>6</sub>H<sub>12</sub>O |
|
|
|
| UNII = 9T7S69J4PS |
| ⚫ |
| MolarMass=100.15888 |
|
|
⚫ |
| PubChem = 11618 |
|
| Appearance= |
|
|
|
| ChEBI_Ref = {{ebicite|correct|EBI}} |
|
| Density= |
|
|
|
| ChEBI = 49106 |
|
| MeltingPt= |
|
|
|
| EINECS = 209-777-2 |
|
| BoilingPt= |
|
|
|
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
|
| Solubility= |
|
|
|
| ChemSpiderID = 11129 |
| ⚫ |
}} |
|
|
⚫ |
| SMILES = C1CCCOCC1 |
| ⚫ |
|Section3={{Chembox Hazards |
|
|
|
| StdInChI_Ref = {{stdinchicite|changed|chemspider}} |
|
| MainHazards= |
|
|
|
| StdInChI = 1S/C6H12O/c1-2-4-6-7-5-3-1/h1-6H2 |
|
| FlashPt= |
|
|
|
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} |
|
| Autoignition= |
|
|
|
| StdInChIKey = UHHKSVZZTYJVEG-UHFFFAOYSA-N |
| ⚫ |
}} |
|
|
⚫ |
}} |
|
|
|
|
⚫ |
| Section2 = {{Chembox Properties |
|
⚫ |
| Formula = C<sub>6</sub>H<sub>12</sub>O |
|
⚫ |
| MolarMass = 100.15888 |
|
|
| Appearance = |
|
|
| Density = |
|
|
| MeltingPt = |
|
|
| BoilingPt = |
|
|
| Solubility = |
|
⚫ |
}} |
|
|
|
|
⚫ |
| Section3 = {{Chembox Hazards |
|
|
| MainHazards = |
|
|
| FlashPt = |
|
|
| AutoignitionPt = |
|
⚫ |
}} |
|
}} |
|
}} |
|
'''Oxepane''' is a ] chemical compound with the ] {{chem|C|6|H|12|O}}. |
|
|
|
|
|
|
|
'''Oxepane''' is a ] chemical compound with the ] C<sub>6</sub>H<sub>12</sub>O: a ] in which one ] is replaced by oxygen.<ref>{{cite web |url=https://pubchem.ncbi.nlm.nih.gov/compound/Oxepane |title=Oxepane (Compound) |author=<!--Not stated--> |date= |website=PubChem |publisher=National Library of Medicine |access-date=May 10, 2020 |quote=}}</ref> |
|
Oxepane can be ]ized by cationic initiators such as {{chem|(C|2|H|5|)|3|OSbCl|6}} to form a crystalline solid with a melting point around 56–58 ].<ref>{{cite journal |
|
|
|
|
|
| title = Ring-opening Polymerization of Oxepane |
|
|
|
Oxepane can be ]ized by cationic initiators such as (C<sub>2</sub>H<sub>5</sub>)<sub>3</sub>OSbCl<sub>6</sub> to form a crystalline solid with a melting point around 56–58 ].<ref>{{cite journal| title = Ring-opening Polymerization of Oxepane| journal = Polymer Journal| volume = 3| year = 1972| issue = 1| pages = 40–43| issn = 1349-0540| author1 = Takeo Saegusa| author2 = Toshiaki Shiota| author3 = Shu-ichi Matsumoto| author4 = Hiroyasu Fujii| DOI=10.1295/polymj.3.40| doi-access = free}}</ref> |
|
| journal = Polymer Journal |
|
|
| volume = 3 |
|
|
| year = 1972 |
|
|
| issue = 1 |
|
|
| pages = 40–43 |
|
|
| issn = 1349-0540 |
|
|
| author1 = Takeo Saegusa |
|
|
| author2 = Toshiaki Shiota |
|
|
| author3 = Shu-ichi Matsumoto |
|
|
| author4 = Hiroyasu Fujii |
|
|
}}</ref> |
|
|
|
|
|
|
==References== |
|
==References== |
| Line 46: |
Line 52: |
|
] |
|
] |
|
|
|
|
|
|
{{heterocyclic-stub}} |
|
|
|
|
{{Organic-compound-stub}} |
|
|
|
|
|
] |
|
|
] |
|
|
] |
|