exo-Norborneol

Names
Preferred IUPAC name

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

Identifiers

CAS Number

* 497-37-0 Y

3D model (JSmol)

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

ChemSpider |

* 9030708 (2R)
* 9215827 (2S)

ECHA InfoCard | 100.007.133

PubChem CID

* 10855417 (2R)
* 11040657 (2S)

UNII |

* V367XM6FYD Y

CompTox Dashboard (EPA)

* DTXSID7022041

InChI

* InChI=1/C7H12O/c8-7-4-5-1-2-6(7)3-5/h5-8H,1-4H2/t5-,6+,7+/s2

Key: ZQTYQMYDIHMKQB-YUZWJPFSNA-N

* (2R): InChI=1S/C7H12O/c8-7-4-5-1-2-6(7)3-5/h5-8H,1-4H2/t5-,6+,7+/m0/s1

Key: ZQTYQMYDIHMKQB-VQVTYTSYSA-N

* (2S): InChI=1S/C7H12O/c8-7-4-5-1-2-6(7)3-5/h5-8H,1-4H2/t5-,6+,7+/m1/s1

Key: ZQTYQMYDIHMKQB-RRKCRQDMSA-N

SMILES

* (2R): O[C@@H]1C[C@@H]2C[C@H]1CC2

* (2S): O[C@H]1C[C@H]2C[C@@H]1CC2

Properties

Chemical formula

| C7H12O
Molar mass | 112.172 g·mol−1
Melting point | 124 to 126 °C (255 to 259 °F; 397 to 399 K)
Boiling point | 176 to 177 °C (349 to 351 °F; 449 to 450 K)
Hazards
Safety data sheet (SDS)  | Fisher MSDS

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Y verify (what is YN ?)

Infobox references

Chemical compound

exo-Norborneol is an alcohol containing the norbornane skeleton. Commercially available, this colorless compound may be prepared by the reaction of norbornene with formic acid, followed by hydrolysis of the resultant exo-norbornyl formate.[1]

## See also[edit]

* Endo-Norborneol

## References[edit]

1. ^ Kleinfelter, Donald C.; von R. Schleyer, Paul (1962). "2-Norbananone". Organic Syntheses. 42: 79. doi:10.15227/orgsyn.042.0079.

## Further reading[edit]

* Reaction of organic compounds under high temperature – dilute acid (HTDA) conditions. III. The perdeuteration of bicyclo[2.2.1]heptanes PDF
* Stille, J. K.; Sonnenberg, Fred M. (1966). "The Reaction of endo- and exo-2-Norborneol with Thionyl Chloride". Journal of the American Chemical Society. 88 (21): 4915. doi:10.1021/ja00973a027.

This article about an alcohol is a stub. You can help Wikipedia by expanding it.

|

* v
* t
* e

*[CID]: Compound ID
*[EPA]: U.S. Environmental Protection Agency
*[v]: View this template
*[t]: Discuss this template
*[e]: Edit this template