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4-oxo-1-iodo-trans-1-octene | 65989-30-2

中文名称
——
中文别名
——
英文名称
4-oxo-1-iodo-trans-1-octene
英文别名
trans-1-Iodo-oct-1en-4one;4-Oxo-1-iod-trans-1-octen;(E)-1-Jod-1-octen-4-on;(E)-1-iodooct-1-en-4-one
4-oxo-1-iodo-trans-1-octene化学式
CAS
65989-30-2
化学式
C8H13IO
mdl
——
分子量
252.095
InChiKey
SWRZXKXCHWOPHU-QPJJXVBHSA-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):
    2.6
  • 重原子数:
    10
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

SDS

SDS:a93943ab6a3cc69441eefcd2f652b748
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反应信息

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文献信息

  • 1-Substituted-1-oxo-prostane-derivatives of the E, A and F series
    申请人:American Cyanamid Company
    公开号:US04297516A1
    公开(公告)日:1981-10-27
    The invention disclosed herein relates to pharmacologically active prostaglandin derivatives of the E, F, or A series having on the terminal methylene carbon of the alpha chain, a substituent selected from the group consisting of: ##STR1## wherein R is C.sub.1 to C.sub.6 alkyl, and phenyl or phenyl substituted with one or more substituents selected from the group consisting of C.sub.1 -C.sub.4 alkyl, OR.sub.16, SR.sub.16, F, or Cl, and R.sub.16 is C.sub.1 to C.sub.6 alkyl.
    本发明公开的药物活性前列腺素生物属于E、F或A系列,在α链的末端亚甲基碳上有一个取代基,该取代基从以下组中选择:##STR1## 其中R是C.sub.1至C.sub.6烷基,和苯基或苯基,苯基上带有1个或多个取代基,该取代基从以下组中选择:C.sub.1-C.sub.4烷基,OR.sub.16,SR.sub.16,F或Cl,R.sub.16是C.sub.1至C.sub.6烷基。
  • 11-(2-Hydroxyethylthio)prostenoic acid E.sub.2 series derivatives
    申请人:American Cyanamid Company
    公开号:US04085272A1
    公开(公告)日:1978-04-18
    This disclosure describes certain 11-(2-hydroxyethylthio)-9-keto-prostenoic acid E series derivatives, and their intermediates, useful as bronchodilators and inflammatory medeator release inhibitors.
    本披露涉及某些11-(2-羟乙基基)-9-酮-前列腺素酸E系列衍生物及其中间体,可用作支气管扩张剂和炎症介质释放抑制剂
  • 1-Hydroxymethyl-1-oxo-prostane-derivatives of the E, A and F-series
    申请人:American Cyanamid Company
    公开号:US04254036A1
    公开(公告)日:1981-03-03
    The invention disclosed herein relates to pharmacologically active prostaglandin derivatives of the E, F, or A series having on the terminal methylene carbon of the alpha chain a substituent selected from the group consisting of: ##STR1## wherein R is an alkyl group and R.sub.15 is C.sub.1 -C.sub.4 alkyl, di-C.sub.1 -C.sub.4 -alkylamino, C.sub.1 -C.sub.4 alkoxy, and phenyl or phenyl substituted with one or more substituents from the group consisting of C.sub.1 -C.sub.4, OR, SR, F, or Cl wherein R is as previously defined.
    本发明涉及具有在α链的末端亚甲基碳上选择自以下组成的取代基的E、F或A系列药理活性前列腺素生物:##STR1##其中R是烷基基团,R.sub.15是C.sub.1 -C.sub.4烷基,二C.sub.1 -C.sub.4-烷基基,C.sub.1 -C.sub.4烷氧基,苯基或苯基,其上取代基来自C.sub.1 -C.sub.4,OR,SR,F或Cl的组成,其中R如前所定义。
  • 1-Hydroxymethyl-1-1-oxo prostane derivatives of the E and F series
    申请人:American Cyanamid Company
    公开号:US04254285A1
    公开(公告)日:1981-03-03
    The invention disclosed herein relates to pharmacologically active prostaglandin derivatives of the E, F, or A series having on the terminal methylene carbon of the alpha chain a substituent selected from the group consisting of: ##STR1## wherein R is an alkyl group and R.sub.15 is C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy, di-C.sub.1 -C.sub.4 -alkylamino, and phenyl orphenyl substituted with one or more substituents selected from the group consisting of C.sub.1 -C.sub.4 alkyl, OR, SR, F, or Cl wherein R is as previously defined.
    本发明涉及具有在α链的末端亚甲基碳上选择自以下组成的取代基的E、F或A系列药理活性前列腺素生物:##STR1## 其中R是烷基基团,R.sub.15是C.sub.1 -C.sub.4烷基,C.sub.1 -C.sub.4烷氧基,二C.sub.1 -C.sub.4-烷基基,以及苯基或苯基取代物,所述苯基或苯基取代物中取代基选择自C.sub.1 -C.sub.4烷基,OR,SR,F或Cl的组成,其中R如前所定义。
  • 11-(2-Hydroxyethylthio) prostenoic acid E and F series derivatives
    申请人:American Cyanamid Company
    公开号:US04218566A1
    公开(公告)日:1980-08-19
    This disclosure describes certain 11-(2-hydroxyethylthio) prostenoic acid E and F series derivatives, and their intermediates, useful as bronchodilators and inflammatory medeator release inhibitors.
    这份披露描述了某些11-(2-羟乙基基)前列腺酸E和F系列衍生物,以及它们的中间体,可用作支气管扩张剂和炎症介质释放抑制剂
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