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词条 Exo-Norborneol
释义

  1. See also

  2. References

  3. Further reading

{{DISPLAYTITLE:exo-Norborneol}}{{chembox
| Watchedfields = changed
| verifiedrevid = 450465653
| Name =exo-Norborneol
| ImageFile =Exo-norborneol 3D-skeletal.png
| ImageSize =
| IUPACName =2-norbornanol
| OtherNames =
|Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|??}}
| CASNo =497-37-0
| PubChem =79028
| SMILES =C1CC2CC1CC2O
|Section2={{Chembox Properties
| C=7 | H=12 | O=1
| Appearance =
| Density =
| MeltingPtC = 124 to 126
| MeltingPt_notes =
| BoilingPtC =176 to 177
| Solubility =
|Section3={{Chembox Hazards
| ExternalSDS = [https://fscimage.fishersci.com/msds/20106.htm Fisher MSDS]
| FlashPt =
| AutoignitionPt =
}}exo-Norborneol is an alcohol containing the norbornane skeleton. Commercially available, this compound may be prepared by the reaction of norbornene with formic acid, followed by hydrolysis of the resultant exo-norbornyl formate.[1]

See also

  • Endo-Norborneol

References

1. ^{{OrgSynth | prep = cv5p0852 | title = 2-Norbananone | author = Donald C. Kleinfelter and Paul von R. Schleyer | collvol = 5 | collvolprep = 852 | year = 1962}}

Further reading

  • Reaction of organic compounds under high temperature – dilute acid (HTDA) conditions. III. The perdeuteration of bicyclo[2.2.1]heptanes [https://web.archive.org/web/20040814160329/http://article.pubs.nrc-cnrc.gc.ca/ppv/RPViewDoc?_handler_=HandleInitialGet PDF]
  • {{cite journal | title = The Reaction of endo- and exo-2-Norborneol with Thionyl Chloride | doi = 10.1021/ja00973a027 | year = 1966 | author = Stille, J. K. | journal = Journal of the American Chemical Society | volume = 88 | pages = 4915 | last2 = Sonnenberg | first2 = Fred M. | issue = 21}}
{{DEFAULTSORT:Norborneol, exo-}}{{alcohol-stub}}

2 : Alcohols|Cyclopentanes

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