1-十七烷醇
外觀
1-十七烷醇[1] | |
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IUPAC名 heptadecan-1-ol | |
別名 | 十七醇,1-十七醇, 正十七醇,正十七烷醇 |
識別 | |
CAS號 | 1454-85-9 ![]() |
PubChem | 15076 |
ChemSpider | 14348 |
SMILES |
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ChEBI | 77470 |
性質 | |
化學式 | C17H36O |
莫耳質量 | 256.5 g·mol⁻¹ |
熔點 | 54.0 °C(327 K) |
沸點 | 309 °C(582 K)[2] |
溶解性(水) | 5.4×10−6 g·L−1(25 °C) |
log P | 8.248[3] |
危險性 | |
閃點 | 155 °C[3] |
相關物質 | |
相關化學品 | 十七烷 |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
1-十七烷醇是一種有機化合物,化學式為C17H36O,是一種難溶於水的脂肪醇。它可以被氧化劑氧化為1-十七醛。[4][5]它和四溴化碳在DMF中加熱反應,可以得到1-溴十七烷。[6]
參考文獻
[編輯]- ^ National Center for Biotechnology Information. 1-Heptadecanol | C17H36O - PubChem. PubChem. National Library of Medicine. [11 March 2021]. (原始內容存檔於6 March 2016).
- ^ Heptadecan-1-ol. Distributed Structure-Searchable Toxicity (DSSTox) Database. United States Environmental Protection Agency. [11 March 2021].
- ^ 3.0 3.1 ChemSpider. MI3885000. [8 March 2021]. (原始內容存檔於28 October 2020).
- ^ Victoria A Brome, Laurence M Harwood, Helen MI Osborn. Preparation of enantiopure long chain threo -2-amino-3-hydroxyesters via chiral morpholinone-derived azomethine ylids. Canadian Journal of Chemistry. 2006-10-01, 84 (10): 1448–1455 [2021-03-17]. ISSN 0008-4042. doi:10.1139/v06-121 (英語).
- ^ Juma'a R. Al-Dulayymi, Mark S. Baird, Hayder Mohammed, Evan Roberts, William Clegg. The synthesis of one enantiomer of the α-methyl-trans-cyclopropane unit of mycolic acids. Tetrahedron. 2006-05, 62 (20): 4851–4862 [2021-03-17]. doi:10.1016/j.tet.2006.03.007. (原始內容存檔於2020-02-22) (英語).
- ^ Terry McCallum, Ekaterina Slavko, Mathieu Morin, Louis Barriault. Light-Mediated Deoxygenation of Alcohols with a Dimeric Gold Catalyst: Light-Mediated Deoxygenation of Alcohols. European Journal of Organic Chemistry. 2015-01, 2015 (1): 81–85 [2021-03-17]. doi:10.1002/ejoc.201403351 (英語).
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