1-三十二烷醇
化合物
1-三十二烷醇是一种有机化合物，化学式为C32H66O。它可由三十二酸甲酯和氢化铝锂在四氢呋喃中反应制得。[3]在三苯基膦存在下，它和N-溴代丁二酰亚胺在二氯甲烷中反应，可以得到1-溴三十二烷。[4]它和乙酸酐反应，得到乙酸三十二烷基酯。[5]
| 1-三十二烷醇 | |
|---|---|
| |
| IUPAC名 Dotriacontan-1-ol | |
| 别名 | 正三十二烷醇 |
| 识别 | |
| CAS号 | 6624-79-9 
|
| PubChem | 96117 |
| ChemSpider | 86761 |
| SMILES |
|
| InChI |
|
| InChIKey | QOEHNLSDMADWEF-UHFFFAOYAH |
| 性质 | |
| 化学式 | C32H66O |
| 摩尔质量 | 466.87 g·mol−1 |
| 熔点 | 89 °C（362 K）[1] 81—82 °C（354—355 K）[2] |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
参考文献
编辑- ^ Sosa, A. Chemical composition of a Mediterranean species of the Ericaceae family, Arbutus unedo. Bulletin de la Societe de Chimie Biologique, 1950. 32: 344-356.
- ^ Mathew, Joseph; George, V. Bioactive compounds from Acrotrema arnottianum. Asian Journal of Chemistry, 2006. 18 (4): 2747-2755.
- ^ Rao, S. Jagadishwar; Bhalerao, U. T.; Tilak, B. D. A new synthesis of long chain acid esters and carbinols. Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1987. 26B (3): 208-211.
- ^ Alexander Scholte, Sebastian Hauche, Matthias Wagner, Marko Prehm, Silvio Poppe, Changlong Chen, Feng Liu, Xiangbing Zeng, Goran Ungar, Carsten Tschierske. A self-assembled liquid crystal honeycomb of highly stretched (3-1-1)-hexagons. Chemical Communications. 2020, 56 (1): 62–65 [2021-11-27]. ISSN 1359-7345. doi:10.1039/C9CC08502E （英语）.
- ^ Euripides G. Stephanou. Analysis of anthropogenic and biogenic lipids in the aerosol of a coastal area in East Mediterranean Sea. Fresenius' Journal of Analytical Chemistry. 1991, 339 (10): 780–784 [2021-11-27]. ISSN 0937-0633. doi:10.1007/BF00321744 （英语）.