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<8-3H>-8-hydroxygeraniol | 69252-86-4

中文名称
——
中文别名
——
英文名称
<8-3H>-8-hydroxygeraniol
英文别名
<10-(3)H>-10-hydroxygeraniol;(2E,6E)-2,6-dimethyl-1-tritioocta-2,6-diene-1,8-diol
<8-3H>-8-hydroxygeraniol化学式
CAS
69252-86-4
化学式
C10H18O2
mdl
——
分子量
172.244
InChiKey
PREUOUJFXMCMSJ-IFXPOFTASA-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):
    1.6
  • 重原子数:
    12
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    <8-3H>-8-hydroxygeraniol 反应 240.0h, 以4.00 mg的产率得到(1S,4aS,7aS)-4-Formyl-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl beta-D-glucopyranoside
    参考文献:
    名称:
    Kobayashi, Koji; Uesato, Shinichi; Ueda, Shinichi, Chemical and pharmaceutical bulletin, 1985, vol. 33, # 10, p. 4228 - 4234
    摘要:
    DOI:
  • 作为产物:
    描述:
    [8-3H]-8-hydroxygeranyl acetate 在 potassium carbonate 作用下, 以 甲醇 为溶剂, 反应 1.0h, 生成 <8-3H>-8-hydroxygeraniol
    参考文献:
    名称:
    The aphid sex pheromone cyclopentanoids: Synthesis in the elucidation of structure and biosynthetic pathways
    摘要:
    Identification of a range of aphid sex pheromones as comprising the cyclopentanoids (4aS,7S,7aR)-nepetalactune, (1R,4aS,7S,7aR)-nepetalactol and the (1S)- and (1R,4aR,7S,7aS)-nepetalactols required samples authenticated by H-1 and C-13 NMR. These and related compounds were provided by small scale synthesis and extraction from plants in the genus Nepeta (Lamiaceae). The subsequent discovery that the synthetic sex pheromones could attract males, and also parasitic wasps that attack aphids, has created a need for large scale syntheses of the cyclopentanoids. This is afforded by cyclisation of the 8-oxo-1-enamine of citronellal as originally developed by Schreiber and co-workers (1986). Investigation into the biosynthesis of the cyclopentanoids by plants for exploiting aphid sex pheromones in crop protection by means of molecular biology required synthesis of putative biosynthetic intermediates, some with radioactive isotopic labelling, particularly 8-oxidised monoterpene alcohols and aldehydes. Copyright (C) 1996 Elsevier Science Ltd
    DOI:
    10.1016/0968-0896(96)00012-0
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