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endo-Norborneol

From Wikipedia, the free encyclopedia
endo-Norborneol[1]
Names
Preferred IUPAC name
rel-(1R,2S,4S)-Bicyclo[2.2.1]heptan-2-ol
Other names
endo-2-Norborneol; endo-Norbornyl alcohol
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.127.627 Edit this at Wikidata
  • InChI=1/C7H12O/c8-7-4-5-1-2-6(7)3-5/h5-8H,1-4H2/t5-,6+,7-/s2
    Key: ZQTYQMYDIHMKQB-HNBBVXEKNA-N
  • (2R): InChI=1S/C7H12O/c8-7-4-5-1-2-6(7)3-5/h5-8H,1-4H2/t5-,6+,7-/m1/s1
    Key: ZQTYQMYDIHMKQB-DSYKOEDSSA-N
  • (2S): InChI=1S/C7H12O/c8-7-4-5-1-2-6(7)3-5/h5-8H,1-4H2/t5-,6+,7-/m0/s1
    Key: ZQTYQMYDIHMKQB-XVMARJQXSA-N
  • (2R): O[C@@H]1C[C@H]2CC[C@@H]1C2
  • (2S): O[C@H]1C[C@@H]2CC[C@H]1C2
Properties
C7H12O
Molar mass 112.17 g/mol
Melting point 149 to 154 °C (300 to 309 °F; 422 to 427 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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endo-Norborneol is an alcohol containing the norbornane skeleton.

See also

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References

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  • endo-Norborneol MSDS
  • Reaction of organic compounds under high temperature – dilute acid (HTDA) conditions. III. The perdeuteration of bicyclo[2.2.1]heptanes PDF
  • J. K. Stille, and Fred M. Sonnenberg (1966). "The Reaction of endo- and exo-2-Norborneol with Thionyl Chloride". J. Am. Chem. Soc. 88 (21): 4915–4921. doi:10.1021/ja00973a027.