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| 177408-59-2

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
177408-59-2
化学式
C14H24O
mdl
——
分子量
208.344
InChiKey
MQWHNGDRIFEVHQ-ARJAWSKDSA-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):
    3.68
  • 重原子数:
    15.0
  • 可旋转键数:
    8.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    20.23
  • 氢给体数:
    1.0
  • 氢受体数:
    1.0

反应信息

  • 作为反应物:
    描述:
    在 lithium aluminium tetrahydride 作用下, 以 二乙二醇二甲醚 为溶剂, 生成 (3E,11Z)-Tetradeca-3,11-dien-1-ol
    参考文献:
    名称:
    Sex pheromone of tomato pestScrobipalpuloides absoluta (Lepidoptera: Gelechiidae)
    摘要:
    The sex attractant of Scrobipalpuloides absoluta females is a 90:10 mixture of (3E,8Z,11Z)-3,8,11-tetradecatrien-1-yl acetate and (3E,8Z)-3,8-tetradecadien-1-yl acetate. Tetradecadienyl acetates bearing 8Z,11Z; 3E,8Z; and 3E,11Z double bonds were synthesized by stereospecific procedures; the mass spectral and gas chromatographic properties of the 3E,8Z isomer were found to be congruent with those of the tetradecadienyl acetate from S. absoluta. In wind tunnel bioassays, a 10:1 mixture of synthetic (3E,8Z,11Z)3,8,11-tetradecatrien-1-yl acetate and (3E,8Z)-3,8-tetradecadien-1-yl acetate was highly attractive to S. absoluta males. Interestingly, the presence of (8Z, 11Z)-8,11-tetradecadien-1-yl acetate (10%) inhibited the response to (3E,8Z,11Z)-3,8,11-tetradecatrien-1-yl acetate completely.
    DOI:
    10.1007/bf02033586
  • 作为产物:
    描述:
    2-[((Z)-Tetradec-11-en-3-ynyl)oxy]-tetrahydro-pyran 在 dowex 50Wx8 作用下, 以 甲醇 为溶剂, 生成
    参考文献:
    名称:
    Sex pheromone of tomato pestScrobipalpuloides absoluta (Lepidoptera: Gelechiidae)
    摘要:
    The sex attractant of Scrobipalpuloides absoluta females is a 90:10 mixture of (3E,8Z,11Z)-3,8,11-tetradecatrien-1-yl acetate and (3E,8Z)-3,8-tetradecadien-1-yl acetate. Tetradecadienyl acetates bearing 8Z,11Z; 3E,8Z; and 3E,11Z double bonds were synthesized by stereospecific procedures; the mass spectral and gas chromatographic properties of the 3E,8Z isomer were found to be congruent with those of the tetradecadienyl acetate from S. absoluta. In wind tunnel bioassays, a 10:1 mixture of synthetic (3E,8Z,11Z)3,8,11-tetradecatrien-1-yl acetate and (3E,8Z)-3,8-tetradecadien-1-yl acetate was highly attractive to S. absoluta males. Interestingly, the presence of (8Z, 11Z)-8,11-tetradecadien-1-yl acetate (10%) inhibited the response to (3E,8Z,11Z)-3,8,11-tetradecatrien-1-yl acetate completely.
    DOI:
    10.1007/bf02033586
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