Names | |
---|---|
Preferred IUPAC name 3-Ethylpentan-3-ol | |
Other names Triethylcarbinol; 1,1-Diethyl-1-propanol; 3-Ethyl-3-hydroxypentane; Triethylmethanol | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ChemSpider | |
ECHA InfoCard | 100.009.003 |
PubChem CID | |
UNII | |
CompTox Dashboard (EPA) | |
InChI
| |
SMILES
| |
Properties | |
Chemical formula | C7H16O |
Molar mass | 116.204 g·mol |
Appearance | Clear liquid |
Density | 0.82 g/cm |
Boiling point | 140–142 °C (284–288 °F; 413–415 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). N verify (what is ?) Infobox references |
3-Ethyl-3-pentanol, also known as 3-ethylpentan-3-ol, is a tertiary alcohol with the molecular formula C7H16O.
It reacts with chromic acid by first dehydrating to an olefin 3-ethyl-2-pentene, and then by converting the double bond to an epoxide.
References
- 3-ethyl-3-pentanol at chemsynthesis.com
- Sager, W. F. (October 1956). "The Chromic Acid Oxidation of 3-Ethyl-3-pentanol". Journal of the American Chemical Society. 78 (19): 4970–4972. doi:10.1021/ja01600a045.
This article about an alcohol is a stub. You can help Misplaced Pages by expanding it. |