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(N->B)phenyl[N(2-methylenebromide)benzylaminodiacetate-O,O',N]borane | 181523-88-6

中文名称
——
中文别名
——
英文名称
(N->B)phenyl[N(2-methylenebromide)benzylaminodiacetate-O,O',N]borane
英文别名
——
(N->B)phenyl[N(2-methylenebromide)benzylaminodiacetate-O,O',N]borane化学式
CAS
181523-88-6
化学式
C18H17BBrNO4
mdl
——
分子量
402.052
InChiKey
FBBMAADQIJRHIW-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

  • 作为反应物:
    描述:
    (N->B)phenyl[N(2-methylenebromide)benzylaminodiacetate-O,O',N]borane甲醇 为溶剂, 以25%的产率得到N-(2-methylenebromide)benzylaminodiacetic acid
    参考文献:
    名称:
    Syntheses of (N → B)phenyl[N-alkylaminodiacetate-O,O′,N]boranes
    摘要:
    The syntheses of (N-->B)phenyl[N-alkylaminodiacetate-O,O',N]boranes (2 to 6) and their corresponding N-alkylaminodiacetic acids (7 to 10) are reported. All compounds (except 6) were characterized by H-1, B-11 (for boron heterocycles), C-13 NMR, infrared spectroscopy and mass spectrometry. The H-1 NMR spectrum of compound 3 shows that it is a chiral molecule, its structure was determined by homonuclear decoupling experiments, H-1 NMR and HETCOR. The study of the intramolecular N-->B coordination by dynamic NMR afforded a Delta G double dagger value of 98.4 kJ mol(-1) for compound 3. Copyright (C) 1996 Elsevier Science Ltd
    DOI:
    10.1016/0277-5387(96)00109-x
  • 作为产物:
    描述:
    (N-B)phenyl[iminodiacetate-O,N]borane1,2-二(溴甲基)苯2,2,6,6-四甲基哌啶正丁基锂 作用下, 以 四氢呋喃正己烷 为溶剂, 以22%的产率得到(N->B)phenyl[N(2-methylenebromide)benzylaminodiacetate-O,O',N]borane
    参考文献:
    名称:
    Syntheses of (N → B)phenyl[N-alkylaminodiacetate-O,O′,N]boranes
    摘要:
    The syntheses of (N-->B)phenyl[N-alkylaminodiacetate-O,O',N]boranes (2 to 6) and their corresponding N-alkylaminodiacetic acids (7 to 10) are reported. All compounds (except 6) were characterized by H-1, B-11 (for boron heterocycles), C-13 NMR, infrared spectroscopy and mass spectrometry. The H-1 NMR spectrum of compound 3 shows that it is a chiral molecule, its structure was determined by homonuclear decoupling experiments, H-1 NMR and HETCOR. The study of the intramolecular N-->B coordination by dynamic NMR afforded a Delta G double dagger value of 98.4 kJ mol(-1) for compound 3. Copyright (C) 1996 Elsevier Science Ltd
    DOI:
    10.1016/0277-5387(96)00109-x
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