endo-Norborneol

endo-Norborneol^[1]

IUPAC name (1R,2S,4S)-Bicyclo[2.2.1]heptan-2-ol (1S,2R,4R)-Bicyclo[2.2.1]heptan-2-ol
Other names endo-2-Norborneol; endo-Norbornyl alcohol
Identifiers
CAS number	61277-90-5^Y, (2R) [36779-79-0] (2S)
PubChem	10975445
ChemSpider	9150646^Y
Jmol-3D images	Image 1 Image 2
SMILES O[C@@H]1C[C@H]2CC[C@@H]1C2 (2S) O[C@H]1C[C@@H]2CC[C@H]1C2 (2R) O[C@H]2C[C@H]1CC[C@@H]2C1
InChI InChI=1S/C7H12O/c8-7-4-5-1-2-6(7)3-5/h5-8H,1-4H2/t5-,6+,7-/m0/s1^Y Key: ZQTYQMYDIHMKQB-XVMARJQXSA-N^Y InChI=1/C7H12O/c8-7-4-5-1-2-6(7)3-5/h5-8H,1-4H2/t5-,6+,7-/m0/s1 Key: ZQTYQMYDIHMKQB-XVMARJQXBK
Properties
Molecular formula	C₇H₁₂O
Molar mass	112.17 g/mol
Melting point	149–154 °C
Y (verify) (what is: Y/N?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

endo-Norborneol is an alcohol.

References

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" (PDF). J. Am. Chem. Soc. 88 (21): 4915–4921. doi:10.1021/ja00973a027. http://pubs.acs.org/doi/abs/10.1021/ja00973a027?journalCode=jacsat&quickLinkVolume=88&quickLinkPage=4915&volume=88.