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[18-13C]linoleic acid

中文名称
——
中文别名
——
英文名称
[18-13C]linoleic acid
英文别名
(9Z,12Z)-(1813C)octadeca-9,12-dienoic acid
[18-13C]linoleic acid化学式
CAS
——
化学式
C18H32O2
mdl
——
分子量
281.44
InChiKey
OYHQOLUKZRVURQ-LFVQVELASA-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

计算性质

  • 辛醇/水分配系数(LogP):
    6.8
  • 重原子数:
    20
  • 可旋转键数:
    14
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.72
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    5-氯戊醛 在 lithium hydroxide 、 硫酸sodium hexamethyldisilazane对甲苯磺酸三氟乙酸 、 sodium iodide 作用下, 以 四氢呋喃二氯甲烷丙酮 为溶剂, 反应 60.1h, 生成 [18-13C]linoleic acid
    参考文献:
    名称:
    Synthesis of [18-11C/(13C)]linoleic acid
    摘要:
    A method for the preparation of [18-C-11]linoleic acid is described. A highly reactive zerovalent copper complex was prepared from lithium (2-thienyl)iodocuprate reduced by lithium naphtalenide. This copper complex was used in a coupling reaction between 17-iodo-cis,cis-9,12-heptadecadienoic acid tert-butyl ester and [C-11]methyl iodide to form [18-C-11]linoleic acid tert-butyl ester as intermediate. The tert-butyl ester protecting group was rapidly removed with trifluoroacetic acid, affording [18-C-11]linoleic acid in 48% radiochemical yield. In a typical run starting with 27 GBq of [C-11]methyl iodide, 2.9 GBq [18-C-11]linoleic acid was obtained within 44 min from the end of radionuclide production.
    DOI:
    10.1002/(sici)1099-1344(199707)39:7<607::aid-jlcr7>3.0.co;2-a
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文献信息

  • Synthesis of [18-11C/(13C)]linoleic acid
    作者:Henrik Neu、Tor Kihlberg、Bengt Långstrom
    DOI:10.1002/(sici)1099-1344(199707)39:7<607::aid-jlcr7>3.0.co;2-a
    日期:1997.7
    A method for the preparation of [18-C-11]linoleic acid is described. A highly reactive zerovalent copper complex was prepared from lithium (2-thienyl)iodocuprate reduced by lithium naphtalenide. This copper complex was used in a coupling reaction between 17-iodo-cis,cis-9,12-heptadecadienoic acid tert-butyl ester and [C-11]methyl iodide to form [18-C-11]linoleic acid tert-butyl ester as intermediate. The tert-butyl ester protecting group was rapidly removed with trifluoroacetic acid, affording [18-C-11]linoleic acid in 48% radiochemical yield. In a typical run starting with 27 GBq of [C-11]methyl iodide, 2.9 GBq [18-C-11]linoleic acid was obtained within 44 min from the end of radionuclide production.
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