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(2E,4E,7Z)-2,4,7-decatrien-1-ol | 157462-02-7

中文名称
——
中文别名
——
英文名称
(2E,4E,7Z)-2,4,7-decatrien-1-ol
英文别名
deca-2t,4c,7c-trien-1-ol;(2E,4Z,7Z)-deca-2,4,7-trien-1-ol
(2E,4E,7Z)-2,4,7-decatrien-1-ol化学式
CAS
157462-02-7
化学式
C10H16O
mdl
——
分子量
152.236
InChiKey
LXIWSTYXFPXANW-OORNVTMFSA-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):
    2.4
  • 重原子数:
    11
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    (2E,4E,7Z)-2,4,7-decatrien-1-olN-氯代丁二酰亚胺二甲基硫 作用下, 生成 (2E,4Z,7Z)-1-Chloro-deca-2,4,7-triene
    参考文献:
    名称:
    Didemnilactones A and B and neodidemnilactone three new fatty acid metabolites isolated from the tunicate Didemnum moseleyi (Herdman)
    摘要:
    Three new fatty acid metabolites didemnilactones A (1) and B (2) and neodidemnilactone (3) were isolated from the tunicate Didemnum moseleyi (Herdman). Their structures including absolute stereochemistry were established on the basis of spectral studies and chemical synthesis. Didemnilactones exhibited inhibitory activity against lipoxygenase and weak binding activity to leukotriene B-4 receptors.
    DOI:
    10.1016/s0040-4020(01)90469-7
  • 作为产物:
    参考文献:
    名称:
    Didemnilactones A and B and neodidemnilactone three new fatty acid metabolites isolated from the tunicate Didemnum moseleyi (Herdman)
    摘要:
    Three new fatty acid metabolites didemnilactones A (1) and B (2) and neodidemnilactone (3) were isolated from the tunicate Didemnum moseleyi (Herdman). Their structures including absolute stereochemistry were established on the basis of spectral studies and chemical synthesis. Didemnilactones exhibited inhibitory activity against lipoxygenase and weak binding activity to leukotriene B-4 receptors.
    DOI:
    10.1016/s0040-4020(01)90469-7
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文献信息

  • A PROCESS FOR THE OXIDATION OF UNSATURATED ALCOHOLS
    申请人:Firmenich SA
    公开号:EP1472207A1
    公开(公告)日:2004-11-03
  • US6995291B2
    申请人:——
    公开号:US6995291B2
    公开(公告)日:2006-02-07
  • [EN] A PROCESS FOR THE OXIDATION OF UNSATURATED ALCOHOLS<br/>[FR] PROCESSUS D'OXYDATION D'ALCOOLS INSATURES
    申请人:FIRMENICH & CIE
    公开号:WO2003064362A1
    公开(公告)日:2003-08-07
    The present invention relates to the field of organic synthesis and more precisely to a process for the synthesis of an unsaturated aldehyde or ketone by oxidation of the corresponding alcohol. Said oxidation is characterized in that it is performed by means of a hypochlorite salt and a catalytic amount of a N-(2,2,6,6-tetraalkyl-4-piperidinyl-N-oxyl)-2-amino-1,3,5-triazine derivative, preferably a N-oxyl derivative of the polymers known under the trademark Chimassorb® 944 or 2020.
  • Didemnilactones A and B and neodidemnilactone three new fatty acid metabolites isolated from the tunicate Didemnum moseleyi (Herdman)
    作者:Haruki Niwa、Masaru Watanabe、Hideaki Inagaki、Kiyoyuki Yamada
    DOI:10.1016/s0040-4020(01)90469-7
    日期:——
    Three new fatty acid metabolites didemnilactones A (1) and B (2) and neodidemnilactone (3) were isolated from the tunicate Didemnum moseleyi (Herdman). Their structures including absolute stereochemistry were established on the basis of spectral studies and chemical synthesis. Didemnilactones exhibited inhibitory activity against lipoxygenase and weak binding activity to leukotriene B-4 receptors.
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