1-三十二烷醇
外观
1-三十二烷醇 | |
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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 |
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InChI |
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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。 |
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]
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).