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Wikipedia

Oxepane

Oxepane is a heterocyclic chemical compound with the formula C6H12O: a cycloheptane in which one methylene group is replaced by oxygen.[1]

Oxepane
Names
Preferred IUPAC name
Oxepane
Other names
Hexamethylene oxide
Identifiers
  • 592-90-5 Y
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:49106 Y
ChemSpider
  • 11129 Y
ECHA InfoCard 100.008.890
EC Number
  • 209-777-2
  • 11618
UNII
  • 9T7S69J4PS Y
  • DTXSID1060471
  • InChI=1S/C6H12O/c1-2-4-6-7-5-3-1/h1-6H2 N
    Key: UHHKSVZZTYJVEG-UHFFFAOYSA-N N
  • C1CCCOCC1
Properties
C6H12O
Molar mass 100.15888
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)

Oxepane can be polymerized by cationic initiators such as (C2H5)3OSbCl6 to form a crystalline solid with a melting point around 56–58 °C.[2]

References

  1. ^ "Oxepane (Compound)". PubChem. National Library of Medicine. Retrieved May 10, 2020.
  2. ^ Takeo Saegusa; Toshiaki Shiota; Shu-ichi Matsumoto; Hiroyasu Fujii (1972). "Ring-opening Polymerization of Oxepane". Polymer Journal. 3 (1): 40–43. doi:10.1295/polymj.3.40. ISSN 1349-0540.

oxepane, heterocyclic, chemical, compound, with, formula, c6h12o, cycloheptane, which, methylene, group, replaced, oxygen, namespreferred, iupac, name, other, names, hexamethylene, oxideidentifierscas, number, model, jsmol, interactive, imagechebi, chebi, 4910. Oxepane is a heterocyclic chemical compound with the formula C6H12O a cycloheptane in which one methylene group is replaced by oxygen 1 Oxepane NamesPreferred IUPAC name OxepaneOther names Hexamethylene oxideIdentifiersCAS Number 592 90 5 Y3D model JSmol Interactive imageChEBI CHEBI 49106 YChemSpider 11129 YECHA InfoCard 100 008 890EC Number 209 777 2PubChem CID 11618UNII 9T7S69J4PS YCompTox Dashboard EPA DTXSID1060471InChI InChI 1S C6H12O c1 2 4 6 7 5 3 1 h1 6H2 NKey UHHKSVZZTYJVEG UHFFFAOYSA N NSMILES C1CCCOCC1PropertiesChemical formula C6H12OMolar mass 100 15888Except where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa N verify what is Y N Infobox references Oxepane can be polymerized by cationic initiators such as C2H5 3OSbCl6 to form a crystalline solid with a melting point around 56 58 C 2 References Edit Oxepane Compound PubChem National Library of Medicine Retrieved May 10 2020 Takeo Saegusa Toshiaki Shiota Shu ichi Matsumoto Hiroyasu Fujii 1972 Ring opening Polymerization of Oxepane Polymer Journal 3 1 40 43 doi 10 1295 polymj 3 40 ISSN 1349 0540 This article about a heterocyclic compound is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Oxepane amp oldid 1105113041, wikipedia, wiki, book, books, library,

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