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(Z)-dec-4-en-1,2-diol | 89616-41-1

中文名称
——
中文别名
——
英文名称
(Z)-dec-4-en-1,2-diol
英文别名
(2RS,4Z)-4-decen-1,2-diol;(Z)-dec-4-ene-1,2-diol
(Z)-dec-4-en-1,2-diol化学式
CAS
89616-41-1
化学式
C10H20O2
mdl
——
分子量
172.268
InChiKey
WBMVOLPFVJEVDJ-SREVYHEPSA-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):
    2.3
  • 重原子数:
    12
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (Z)-dec-4-en-1,2-diollead(IV) acetate 作用下, 以 二氯甲烷 为溶剂, 生成 (Z)-壬-3-烯醛
    参考文献:
    名称:
    Irreversible inhibition of prostaglandin and leukotriene biosynthesis from arachidonic acid by 11,12-dehydro- and 5,6-dehydroarachidonic acids, respectively
    摘要:
    DOI:
    10.1021/ja00370a058
  • 作为产物:
    描述:
    2,2-dimethyl-4-[(Z)-oct-2-enyl]-1,3-dioxolane溶剂黄146 作用下, 反应 20.0h, 以92%的产率得到(Z)-dec-4-en-1,2-diol
    参考文献:
    名称:
    Synthesis of the Eight Enantiomerically Pure Diastereomers of the 12-F2-Isoprostanes
    摘要:
    Syntheses of the eight enantiomerically pure diastereomers of the 12-F-2-isoprostanes (4-11) are described. The key steps included rhodium-mediated intramolecular cyclopropanation and enzymatic resolution of the racemic diol 12.
    DOI:
    10.1021/ja020816v
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文献信息

  • Absolute configuration of C(1)C(5) fragment of AAL-toxin: Conformationally rigid acyclic aminotriol moiety
    作者:Hideaki Oikawa、Isamu Matsuda、Akitami Ichihara、Keisuke Kohmoto
    DOI:10.1016/0040-4039(94)88029-8
    日期:1994.2
    Degradation of AAL-toxin 1 a host-specific phytotoxin and synthesis of model aminotriol 7a - 7d allowed us to determine the absolute configuration of C(1)C(5) fragment as 2S, 4S and 5R. Unusually rigid conformation of this acyclic fragment was also discussed.
    AAL-毒素降解1宿主特异性植物毒素和模型aminotriol的合成图7a - 7D使我们能够确定C的绝对构型(1)C(5)片段作为2小号,4小号和5 - [R 。还讨论了该无环片段的异常刚性构象。
  • An efficient preparation of stereospecific β-hydroxy nitriles
    作者:Sheila H. Jacobo、Mustafa Adiyaman、Chih-Tsung Chang、Nam-In Kang、William S. Powell、Joshua Rokach
    DOI:10.1016/j.tetlet.2004.10.174
    日期:2005.1
    The cyanide-ring opening of thionocarbonates with NaCN in DMF and TBACN in THF is described. This reaction occurred regioselectively to afford β-hydroxy nitrile with preserved stereochemistry of the hydroxy group in high yield.
    描述了在DMF中用NaCN和在THF中用TBACN对硫代碳酸酯的氰化物环的开环。该反应选择性地发生,从而以高收率提供了具有保留的羟基立体化学的β-羟基腈。
  • Absolute configuration of main chain of AAL-toxins.
    作者:Hideaki Oikawa、Isamu Matsuda、Takashi Kagawa、Akitami Ichihara、Keisuke Kohmoto
    DOI:10.1016/s0040-4020(01)89343-1
    日期:1994.1
    AAL-toxins TA(1) 1 and TA(2) 2, host-specific toxins produced by Alternaria alternata, were degraded to 2-methylbutanol, 3-methylnonan-1,9-diol and N-protected 4-aminobutan-1-3-diol, which were further converted to (R)-MTPA esters. These esters were correlated with synthesis samples by comparison of their 500 MHz H-1-NMR spectra. The remaining stereocenters were determined by the comparison of H-1-NMR spectra of 6a and 7 derived from 1 and 2 with those of synthetic model compounds. These data conclude that AAL-toxins possess 2S, 4S, 5R, 11S, 13S, 14R and 15R configurations.
  • Irreversible inhibition of prostaglandin and leukotriene biosynthesis from arachidonic acid by 11,12-dehydro- and 5,6-dehydroarachidonic acids, respectively
    作者:E. J. Corey、John E. Munroe
    DOI:10.1021/ja00370a058
    日期:1982.3
  • Stereochemical course of 5-lipoxygenation of arachidonate by rat basophil leukemic cell (RBL-1) and potato enzymes
    作者:E. J. Corey、Peter T. Lansbury
    DOI:10.1021/ja00350a059
    日期:1983.6
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