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7,7,7-trifluoro-hepta-1,5-dien-4-ol | 1234064-03-9

中文名称
——
中文别名
——
英文名称
7,7,7-trifluoro-hepta-1,5-dien-4-ol
英文别名
(5E)-7,7,7-trifluorohepta-1,5-dien-4-ol
7,7,7-trifluoro-hepta-1,5-dien-4-ol化学式
CAS
1234064-03-9
化学式
C7H9F3O
mdl
——
分子量
166.143
InChiKey
HBWLSVQOLMKZFS-SNAWJCMRSA-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):
    2.1
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    7,7,7-trifluoro-hepta-1,5-dien-4-ol丙烯酰氯4-二甲氨基吡啶三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 6.0h, 以60%的产率得到acrylic acid 1-allyl-4,4,4-trifluoro-but-2-enyl ester
    参考文献:
    名称:
    Synthesis and cytotoxic activity of fluorinated analogues of Goniothalamus lactones. Impact of fluorine on oxidative processes
    摘要:
    Novel fluorinated analogues of goniothalamin 1 and howiinol A 2 have been prepared from trifluorocrotonate derivatives. Trifluoromethyl goniothalamin (R/S) 4 showed a slightly lower activity than 1, while the trifluoromethyl howiinol A 16 exhibited similar activities on several cell lines in the micromolar range. Unlike (R) goniothalamin and howiinol A, trifluoromethyl parent compounds remained unchanged when submitted to biomimetic oxidative systems. (C) 2010 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2010.03.032
  • 作为产物:
    描述:
    (E)-4,4,4-trifluorobut-2-enal3-溴丙烯三甲基氯硅烷氯化铵 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 4.0h, 以2.1 g的产率得到7,7,7-trifluoro-hepta-1,5-dien-4-ol
    参考文献:
    名称:
    Synthesis and cytotoxic activity of fluorinated analogues of Goniothalamus lactones. Impact of fluorine on oxidative processes
    摘要:
    Novel fluorinated analogues of goniothalamin 1 and howiinol A 2 have been prepared from trifluorocrotonate derivatives. Trifluoromethyl goniothalamin (R/S) 4 showed a slightly lower activity than 1, while the trifluoromethyl howiinol A 16 exhibited similar activities on several cell lines in the micromolar range. Unlike (R) goniothalamin and howiinol A, trifluoromethyl parent compounds remained unchanged when submitted to biomimetic oxidative systems. (C) 2010 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2010.03.032
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文献信息

  • Synthesis and cytotoxic activity of fluorinated analogues of Goniothalamus lactones. Impact of fluorine on oxidative processes
    作者:Lidia Dumitrescu、Doan Thi Mai Huong、Nguyen Van Hung、Benoit Crousse、Danièle Bonnet-Delpon
    DOI:10.1016/j.ejmech.2010.03.032
    日期:2010.7
    Novel fluorinated analogues of goniothalamin 1 and howiinol A 2 have been prepared from trifluorocrotonate derivatives. Trifluoromethyl goniothalamin (R/S) 4 showed a slightly lower activity than 1, while the trifluoromethyl howiinol A 16 exhibited similar activities on several cell lines in the micromolar range. Unlike (R) goniothalamin and howiinol A, trifluoromethyl parent compounds remained unchanged when submitted to biomimetic oxidative systems. (C) 2010 Elsevier Masson SAS. All rights reserved.
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