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5-(trifluoromethyl)-5-nonanol | 118143-26-3

中文名称
——
中文别名
——
英文名称
5-(trifluoromethyl)-5-nonanol
英文别名
5-(Trifluoromethyl)nonan-5-ol
5-(trifluoromethyl)-5-nonanol化学式
CAS
118143-26-3
化学式
C10H19F3O
mdl
——
分子量
212.255
InChiKey
PYBJLFPHXOGVCB-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    228.1±35.0 °C(Predicted)
  • 密度:
    1.022±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.1
  • 重原子数:
    14
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    5-壬酮四丁基氟化铵 盐酸 作用下, 以 四氢呋喃 为溶剂, 反应 27.0h, 生成 5-(trifluoromethyl)-5-nonanol
    参考文献:
    名称:
    Synthetic methods and reactions. 141. Fluoride-induced trifluoromethylation of carbonyl compounds with trifluoromethyltrimethylsilane (TMS-CF3). A trifluoromethide equivalent
    摘要:
    DOI:
    10.1021/ja00183a073
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文献信息

  • Preparation of trifluoromethyl and other perfluoroalkyl compounds with (perfluoroalkyl)trimethylsilanes
    作者:Ramesh Krishnamurti、Donald R. Bellew、G. K. Surya Prakash
    DOI:10.1021/jo00003a017
    日期:1991.2
    The preparation of a variety of novel perfluoroalkyl-substituted compounds in high yields using easily prepared (perfluoroalkyl)trimethylsilanes (1a-c) is described. (Trifluoromethyl)-, (pentafluoroethyl)-, and (heptafluoropropyl)trimethylsilane, 1a-c, respectively, react readily with carbonyl compounds, such as aldehydes and ketones, by a fluoride-initiated catalytic process. Fluoride-initiated addition of 1 to a carbonyl group generates an oxyanionic species which then further catalyzes the reaction. Even enolizable carbonyl compounds react cleanly under the reaction conditions. A study of the scope of the reactivity of 1a toward other carbonyl groups in esters, lactones and an acid chloride was also carried out. Thus 1a reacts cleanly with five- and six-membered ring lactones. However, unactivated esters do not react under the reaction conditions. The acid chloride reacts with 1a to give a mixture of products.
  • PRAKASH, G. K. SURYA;KRISHNAMURTI, RAMESH;OLAH, GEORGE A., J. AMER. CHEM. SOC., 111,(1989) N, C. 393-395
    作者:PRAKASH, G. K. SURYA、KRISHNAMURTI, RAMESH、OLAH, GEORGE A.
    DOI:——
    日期:——
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