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(1-bromoprop-1-en-2-yl)cyclohexane | 90721-89-4

中文名称
——
中文别名
——
英文名称
(1-bromoprop-1-en-2-yl)cyclohexane
英文别名
(1-Bromoprop-1-en-2-yl)cyclohexane;1-bromoprop-1-en-2-ylcyclohexane
(1-bromoprop-1-en-2-yl)cyclohexane化学式
CAS
90721-89-4
化学式
C9H15Br
mdl
——
分子量
203.122
InChiKey
MCULJCSPETVXLN-UHFFFAOYSA-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):
    4.6
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.78
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

点击查看最新优质反应信息

文献信息

  • PYRIDO[4,3-B]INDOLES CONTAINING RIGID MOIETIES
    申请人:HUNG David T.
    公开号:US20100216814A1
    公开(公告)日:2010-08-26
    This disclosure is directed to pyrido[4,3-b]indoles having rigid moieties. The compounds in one embodiment are pyrido[4,3-b]indoles having an unsaturated hydrocarbon moiety. The compounds in another embodiment are pyrido[4,3-b]indoles having a cycloalkyl, cycloalkenyl or heterocyclyl moiety. Pharmaceutical compositions comprising the compounds are also provided, as are methods of using the compounds in a variety of therapeutic applications, including the treatment of a cognitive disorder, psychotic disorder, neurotransmitter-mediated disorder and/or a neuronal disorder.
    本文揭示了具有刚性基团的吡啶并[4,3-b]吲哚。在一种实施例中,化合物是具有不饱和碳氢基团的吡啶并[4,3-b]吲哚。在另一种实施例中,化合物是具有环烷基,环烯基或杂环基团的吡啶并[4,3-b]吲哚。还提供了包括这些化合物的制药组合物,以及使用这些化合物进行各种治疗应用的方法,包括治疗认知障碍,精神障碍,神经递质介导的障碍和/或神经元障碍。
  • Pyrido[4,3-B]indoles containing rigid moieties
    申请人:Medivation Technologies, Inc.
    公开号:US08906925B2
    公开(公告)日:2014-12-09
    This disclosure is directed to pyrido[4,3-b]indoles having rigid moieties. The compounds in one embodiment are pyrido[4,3-b]indoles having an unsaturated hydrocarbon moiety. The compounds in another embodiment are pyrido[4,3-b]indoles having a cycloalkyl, cycloalkenyl or heterocyclyl moiety. Pharmaceutical compositions comprising the compounds are also provided, as are methods of using the compounds in a variety of therapeutic applications, including the treatment of a cognitive disorder, psychotic disorder, neurotransmitter-mediated disorder and/or a neuronal disorder.
    本公开涉及具有刚性基团的吡啶并[4,3-b]吲哚。在一种实施例中,化合物是具有不饱和碳氢基团的吡啶并[4,3-b]吲哚。在另一种实施例中,化合物是具有环烷基,环烯基或杂环基团的吡啶并[4,3-b]吲哚。还提供了包含该化合物的制药组合物,以及使用该化合物在多种治疗应用中的方法,包括治疗认知障碍,精神疾病,神经递质介导的疾病和/或神经元疾病。
  • Pyrido[4,3-b]indoles containing rigid moieties
    申请人:Hung David T.
    公开号:US08907097B2
    公开(公告)日:2014-12-09
    This disclosure is directed to pyrido[4,3-b]indoles having rigid moieties. The compounds in one embodiment are pyrido[4,3-b]indoles having an unsaturated hydrocarbon moiety. The compounds in another embodiment are pyrido[4,3-b]indoles having a cycloalkyl, cycloalkenyl or heterocyclyl moiety. Pharmaceutical compositions comprising the compounds are also provided, as are methods of using the compounds in a variety of therapeutic applications, including the treatment of a cognitive disorder, psychotic disorder, neurotransmitter-mediated disorder and/or a neuronal disorder.
    本公开涉及具有刚性基团的吡啶并[4,3-b]吲哚。在一种实施例中,化合物是具有不饱和碳氢基团的吡啶并[4,3-b]吲哚。在另一种实施例中,化合物是具有环烷基、环烯基或杂环基团的吡啶并[4,3-b]吲哚。还提供了包括这些化合物的药物组合物,以及使用这些化合物在各种治疗应用中的方法,包括治疗认知障碍、精神疾病、神经递质介导的疾病和/或神经元疾病。
  • Bromoform Activation. TiCl<sub>4</sub>–Mg-Promoted CHBr<sub>2</sub><sup>–</sup> and CBr<sub>3</sub><sup>–</sup> Transfer to a Variety of Aldehydes and Ketones
    作者:Tu-Hsin Yan、Su-Haur Chang、Cheng-Ta Chang、Chia-Kuan Lin、Chien-Yu Liu
    DOI:10.1021/ol402861a
    日期:2013.11.15
    TiCl4-Mg can mediate addition of CHBr3 to a variety of aldehydes and ketones to form dibromomethyl carbinols and also be used to effect CBr3 transfer to carbonyl groups to form tribromomethyl carbinols. The successful application of TiCl4-Mg-promoted coupling of CHBr3 with various carbonyl compounds, especially in the case of highly enolizable ketones such as 2-indanone and beta-tetralone, highlights the extraordinary reactivity and selectivity and the weakly basic nature of this system.
  • An Enantioselective Aminocatalytic Cascade Reaction Affording Bioactive Hexahydroazulene Scaffolds
    作者:Jonas Faghtmann、Macarena Eugui、Johannes Nygaard Lamhauge、Signe Sofie Pladsbjerg Andresen、Anne Rask Østergaard、Esben Bjerregaard Svenningsen、Thomas B. Poulsen、Karl Anker Jørgensen
    DOI:10.1002/chem.202401156
    日期:——
    Organocatalysis opens up for a novel cascade reaction concept where 3-oxidopyridinium betaines first undergo an enantioselective [6+4] cycloaddition with trienamines, followed by a spontaneously series of reactions to provide chiral hexahydraoazulenes, of which some show bioactivity.
    有机催化开辟了一种新的级联反应概念,其中3-氧化吡啶鎓甜菜碱首先与三烯胺进行对映选择性[6+4]环加成,随后发生一系列自发反应,得到手性六氢薁蓝烯,其中一些显示出生物活性。
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