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3,8,9,10,12-I5-1,2-closo-C2B10H7 | 1046142-54-4

中文名称
——
中文别名
——
英文名称
3,8,9,10,12-I5-1,2-closo-C2B10H7
英文别名
——
3,8,9,10,12-I5-1,2-closo-C2B10H7化学式
CAS
1046142-54-4
化学式
C2H7B10I5
mdl
——
分子量
773.71
InChiKey
KQCLSEXLHASVBG-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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为产物:
    描述:
    3-iodo-o-carborane 以 neat (no solvent) 为溶剂, 以79%的产率得到3,8,9,10,12-I5-1,2-closo-C2B10H7
    参考文献:
    名称:
    Designed Synthesis of New ortho-Carborane Derivatives: from Mono- to Polysubstituted Frameworks
    摘要:
    The use of nucleophilic and electrophilic processes allow the designed synthesis of several B-iodinated derivatives of o-carborane. Because of the straightforward Pd-catalyzed conversion of B-I to B-C bond with Grignard reagents, such as methylMgBr and biPhenylMgBr, both, symmetrical 3,6-R-2-1,2-closo-C2B10H10 and asymmetrical 3-1-6-Me-1,2-closo-C2B10H10 could be obtained. Not only conventional reactions in solution have been studied but also a highly efficient, clean and fast solvent-free procedure has provided successful results to regioselectively produce B-iodinated o-carborane derivatives by a careful control of the reaction conditions. The high number of nonequivalent leaving groups in boron iodinated o-carborane derivatives opens the possibility through B-C coupling to materials with novel possibilities and to self-assembling due to the enhanced polarizability of the C-H bond.
    DOI:
    10.1021/ic800362z
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