1-十七烷醇

化合物

1-十七烷醇是一种有机化合物,化学式为C17H36O,是一种难溶于水的脂肪醇。它可以被氧化剂氧化为1-十七醛。[4][5]它和四溴化碳DMF中加热反应,可以得到1-溴十七烷[6]

1-十七烷醇[1]
Structural model of 1-heptadecanol
Space-filling model of 1-heptadecanol
IUPAC名
heptadecan-1-ol
别名 十七醇,1-十七醇,
正十七醇,正十七烷醇
识别
CAS号 1454-85-9  checkY
PubChem 15076
ChemSpider 14348
SMILES
 
  • CCCCCCCCCCCCCCCCCO
ChEBI 77470
性质
化学式 C17H36O
摩尔质量 256.5 g·mol⁻¹
熔点 54.0 °C(327 K)
沸点 309 °C(582 K)[2]
溶解性 5.4×10−6 g·L−1(25 °C)
log P 8.248[3]
危险性
闪点 155 °C[3]
相关物质
相关化学品 十七烷
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。

参考文献

  1. ^ National Center for Biotechnology Information. 1-Heptadecanol | C17H36O - PubChem. PubChem. National Library of Medicine. [11 March 2021]. (原始内容存档于6 March 2016). 
  2. ^ Heptadecan-1-ol. Distributed Structure-Searchable Toxicity (DSSTox) Database. United States Environmental Protection Agency. [11 March 2021]. 
  3. ^ 3.0 3.1 ChemSpider. MI3885000. [8 March 2021]. (原始内容存档于28 October 2020). 
  4. ^ 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 (英语). 
  5. ^ 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. (原始内容存档于2020-02-22) (英语). 
  6. ^ 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 (英语).