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| 1537877-82-9

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1537877-82-9
化学式
C8H15I
mdl
——
分子量
238.112
InChiKey
GCCFHHREIHRJQH-ZKCHVHJHSA-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

物化性质

  • 沸点:
    224.7±9.0 °C(Predicted)
  • 密度:
    1.431±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.25
  • 重原子数:
    9.0
  • 可旋转键数:
    1.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0.0
  • 氢给体数:
    0.0
  • 氢受体数:
    0.0

反应信息

  • 作为产物:
    描述:
    (4-甲基环己-3-烯-1-基)甲醇咪唑叔丁基过氧化氢 、 Mn(dpm)3苯硅烷三苯基膦 作用下, 以 癸烷二氯甲烷异丙醇 为溶剂, 反应 0.75h, 生成
    参考文献:
    名称:
    Simple, Chemoselective Hydrogenation with Thermodynamic Stereocontrol
    摘要:
    Few methods permit the hydrogenation of alkenes to a thermodynamically favored configuration when steric effects dictate the alternative trajectory of hydrogen delivery. Dissolving metal reduction achieves this control, but with extremely low functional group tolerance. Here we demonstrate a catalytic hydrogenation of alkenes that affords the thermodynamic alkane products with remarkably broad functional group compatibility and rapid reaction rates at standard temperature and pressure.
    DOI:
    10.1021/ja412342g
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文献信息

  • VLA-4 INHIBITORY DRUG
    申请人:Daiichi Sankyo Company, Limited
    公开号:EP1961750B1
    公开(公告)日:2013-09-18
  • [EN] FIVE-MEMBERED HETEROCYCLES USEFUL AS SERINE PROTEASE INHIBITORS<br/>[FR] HETEROCYCLES A CINQ CHAINONS UTILISES COMME INHIBITEURS DE LA SERINE PROTEASE
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2005123050A2
    公开(公告)日:2005-12-29
    The present invention provides a method for treating a thrombotic or an inflammatory disorder administering to a patient in need thereof a therapeutically effective amount of at least one compound of Formula (I) or Formula (V): (I) [INSERTCHEMICAL STRUCTURE HERE] (V)[INSERT CHEMICAL STRUCTURE HERE] or a stereoisomer or pharmaceutically acceptable salt or solvate form thereof, wherein the variables A, L, Z, R3, R4, R6, R11, X1, X2, and X3 are as defined herein. The compounds of Formula (I) are useful as selective inhibitors of serine protease enzymes of the coagulation cascade and/or contact activation system; for example thrombin, factor Xa, factor XIa, factor IXa, factor VIIa and/or plasma kallikrein. In particular, it relates to compounds that are selective factor XIa inhibitors. This invention also provides compounds within the scope of Formula I and relates to pharmaceutical compositions comprising these compounds.
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