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7,7-dibromobicyclo[4.1.0]heptane-3,4-diol | 669051-41-6

中文名称
——
中文别名
——
英文名称
7,7-dibromobicyclo[4.1.0]heptane-3,4-diol
英文别名
——
7,7-dibromobicyclo[4.1.0]heptane-3,4-diol化学式
CAS
669051-41-6
化学式
C7H10Br2O2
mdl
——
分子量
285.963
InChiKey
RCRSOGJNJGPYGZ-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

物化性质

  • 熔点:
    142-144 °C
  • 沸点:
    320.2±42.0 °C(Predicted)
  • 密度:
    2.263±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.3
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Practical synthesis of biaryl colchicinoids containing 3′,4′-catechol ether-based A-rings via Suzuki cross-coupling with ligandless palladium in water
    摘要:
    Eight new biaryl colchicinoids containing 3',4'-methylene or benzodioxy ether bridges were synthesized. The key synthetic step employed a ligandless, aqueous Suzuki cross-coupling reaction catalyzed by Pd(OAc)(2) with tetrabutylammonium bromide (TBAB) and potassium carbonate (K2CO3). The biaryl Suzuki products were typically formed in 5-30 min and always in less than 1 h. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2003.11.016
  • 作为产物:
    描述:
    7,7-二溴-二环[4.1.0]庚-3-烯四氧化锇异丁醇N-甲基吗啉氧化物 作用下, 以 丙酮叔丁醇 为溶剂, 以72%的产率得到7,7-dibromobicyclo[4.1.0]heptane-3,4-diol
    参考文献:
    名称:
    Practical synthesis of biaryl colchicinoids containing 3′,4′-catechol ether-based A-rings via Suzuki cross-coupling with ligandless palladium in water
    摘要:
    Eight new biaryl colchicinoids containing 3',4'-methylene or benzodioxy ether bridges were synthesized. The key synthetic step employed a ligandless, aqueous Suzuki cross-coupling reaction catalyzed by Pd(OAc)(2) with tetrabutylammonium bromide (TBAB) and potassium carbonate (K2CO3). The biaryl Suzuki products were typically formed in 5-30 min and always in less than 1 h. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2003.11.016
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文献信息

  • WO2019200314A5
    申请人:——
    公开号:WO2019200314A5
    公开(公告)日:2022-04-15
  • HINOKITIOL ANALOGUES, METHODS OF PREPARING AND PHARMACEUTICAL COMPOSITIONS THEREOF
    申请人:The Board of Trustees of the University of Illinois
    公开号:EP3773900A2
    公开(公告)日:2021-02-17
  • [EN] HINOKITIOL ANALOGUES, METHODS OF PREPARING AND PHARMACEUTICAL COMPOSITIONS THEREOF<br/>[FR] ANALOGUES D'HINOKITIOL, PROCÉDÉS DE PRÉPARATION ET COMPOSITIONS PHARMACEUTIQUES DE CEUX-CI
    申请人:UNIV ILLINOIS
    公开号:WO2019200314A2
    公开(公告)日:2019-10-17
    Disclosed are analogues of hinokitiol, methods for preparing them, and pharmaceutical compositions thereof. Also disclosed are methods for their use in treating iron-related diseases.
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