endo-Norborneol

endo -Norborneol

Names

Preferred IUPAC name rel-(1R,2S,4S)-Bicyclo[2.2.1]heptan-2-ol

Other names endo-2-Norborneol; endo-Norbornyl alcohol

Identifiers

CAS Number(2R)Y(2S)N

3D model ( JSmol )(2R):(2S):

ChemSpider(2R)(2S)Y

ECHA InfoCard

PubChem CID(2R)(2S)

InChI InChI=1/C7H12O/c8-7-4-5-1-2-6(7)3-5/h5-8H,1-4H2/t5-,6+,7-/s2Key: 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/s1Key: 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/s1Key: ZQTYQMYDIHMKQB-XVMARJQXSA-N

SMILES (2R): O[C@@H]1C[C@H]2CC[C@@H]1C2(2S): O[C@H]1C[C@@H]2CC[C@H]1C2

Properties

Chemical formulaC7H12O

Molar mass112.17 g/mol

Melting point149 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). N verify (what is YN ?) Infobox references

endo-Norborneol is an alcohol containing the norbornane skeleton.

External links

Reaction of organic compounds under high temperature – dilute acid (HTDA) conditions. III. The perdeuteration of bicyclo[2.2.1]heptanes
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. Bibcode:. doi:.

endo-Norborneol

See also

External links