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(3R)-1-methoxy-3-methylcyclopentane

中文名称
——
中文别名
——
英文名称
(3R)-1-methoxy-3-methylcyclopentane
英文别名
——
(3R)-1-methoxy-3-methylcyclopentane化学式
CAS
——
化学式
C7H14O
mdl
——
分子量
114.19
InChiKey
DSQVNZQPDSIEBT-ULUSZKPHSA-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):
    1.8
  • 重原子数:
    8
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

文献信息

  • [EN] SUBSTITUTED XANTHINES AND METHODS OF USE THEREOF<br/>[FR] XANTHINES SUBSTITUÉES ET LEURS MÉTHODES D'UTILISATION
    申请人:HYDRA BIOSCIENCES INC
    公开号:WO2014143799A2
    公开(公告)日:2014-09-18
    Compounds, compositions and methods are described for inhibiting the TRPC5 ion channel and disorders related to TRPC5.
    描述了抑制TRPC5离子通道及与TRPC5相关的疾病的化合物、组合物和方法。
  • Methods Of Making Fused Ring Compounds
    申请人:Transitions Optical, Inc.
    公开号:US20150336922A1
    公开(公告)日:2015-11-26
    The present invention relates to methods of making fused ring compounds, such as indeno-fused naphthols, and fused ring indenopyran compounds, such as indeno-fused naphthopyrans, that each employ an unsaturated compound represented by the following Formula II. Referring to the unsaturated compound of Formula II: Ring-A can be selected from optionally substituted aryl (e.g., phenyl); m can be, for example, from 0 to 4; R 1 for each m can be selected from optionally substituted hydrocarbyl (e.g., C 1 -C 6 alkyl) optionally interrupted with at least one linking group (e.g., —O—); and R 3 and R 16 can each be independently selected from, for example, hydrogen or optionally substituted hydrocarbyl, such as C 1 -C 8 alkyl. When Ring-A is a phenyl group, the unsaturated compound represented by Formula II can be referred to as an unsaturated indanone acid/ester compound, or an indenone acid/ester compound (depending on whether R 16 is hydrogen, or an optionally substituted hydrocarbyl group).
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