Endo-Norborneol

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

CAS Number

* 61277-90-5 (2R) Y
* 36779-79-0 (2S) N

3D model (JSmol)

* (2R): Interactive image
* (2S): Interactive image

ChemSpider |

* 9030707 (2R)
* 9150646 (2S) Y

PubChem CID

* 10855416 (2R)
* 10975445 (2S)

InChI

* 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

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 formula

| 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).

N verify (what is YN ?)
Infobox references

endo-Norborneol is an alcohol.

## See also

* Exo-Norborneol

## References

1. ↑ (+)-endo-2-Norborneol at Sigma-Aldrich

## External links

* 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.

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*[CID]: Compound ID