1.9-Dihydroperfluor-5-nonanon | 755-64-6

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1.9-Dihydroperfluor-5-nonanon
• 英文别名: 1.9-H2-Hexadecafluor-nonanon-(5)；1H,9H-hexadecafluoro-nonan-5-one；1,1,2,2,3,3,4,4,6,6,7,7,8,8,9,9-Hexadecafluorononan-5-one；1,1,2,2,3,3,4,4,6,6,7,7,8,8,9,9-hexadecafluorononan-5-one
• CAS: 755-64-6
• 化学式: C₉H₂F₁₆O
• 分子量: 430.089
• InChiKey: WXTGITZIMZPFAY-UHFFFAOYSA-N

物化性质

• 沸点：
  147 °C
• 密度：
  1.638±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.7
• 重原子数：
  26
• 可旋转键数：
  8
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.89
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  17

反应信息

• 作为产物：
  描述：

  5H-八氟氯戊醇 在 tetracarbonyl nickel 作用下， 反应 4.0h， 生成 1H,8H-全氟辛烷 、 1.9-Dihydroperfluor-5-nonanon
  参考文献：
  名称：

  Syntheses by Free-Radical Reactions. XII. Reactions of Fluoroacyl Radicals

  摘要：

  DOI：

  10.1021/ja01504a025

文献信息

• [EN] FLUORINATED KETONE AND FLUORINATED ETHERS AS WORKING FLUIDS FOR THERMAL ENERGY CONVERSION<br/>[FR] CETONE FLUOREE ET ETHERS FLUORES COMME FLUIDES DE TRAVAIL POUR LA CONVERSION DE L'ENERGIE THERMIQUE
  申请人：HONEYWELL INT INC

  公开号：WO2005085398A2

  公开（公告）日：2005-09-15

  Polyfluorinated ethers and polyfluorinated ketones and mixtures thereof, preferably polyfluorinated ethers such as methyl (trifluoroethyl) ether (CH3OCH2CF3), methyl (heptafluoropropyl) ether (CH3OCF2CHFCF3), di(trifluoroethyl) ether (CF3CH2OCH2CF3), methyl (hexafluoropropyl) ether (CH3OCF2CF2CHF2), methyl (pentafluoropropyl) ether (CH3OCH2CF2CF3), methyl (perfluorobutyl) ether (C4F9OCH3), ethyl (perfluorobutyl) ether (C4F9OC2H5), and polyfluorinated ketones such as methyl (perfluoromethyl) ketone (CF3COCH3), perfluoromethyl (trifluoroethyl) ketone (CF3CH2COCF3), methyl (perfluooroethyl) ketone (C2F5COCH3), methyl (perfluoropropyl) ketone (F3CF2CF2COCH3), perfluoroethyl (perfluoropropyl) ketone (CF3CF2CF2COC2F5), methyl (octafluorobutyl) ketone (C2F5CFHCF2COCH3), di(perfluoropropyl) ketone (CF3CF2CF2COCF2CF2CF3), and mixtures thereof meet the requirement for not adversely affect atmospheric chemistry and would be a negligible contributor to ozone depletion and to green-house global warming in comparison to the fully halogenated hydrocarbons and are suitable for use as working fluids for u se i n thermal energy conversion systems such as an organic Rankine cycle system.
• Syntheses by Free-Radical Reactions. XII. Reactions of Fluoroacyl Radicals
  作者：J. J. Drysdale、Donald D. Coffman

  DOI：10.1021/ja01504a025

  日期：1960.10