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5-((4-methoxyphenyl)diazenyl)-6-methyl-2,2,6-triphenyl-3H-1,3,2λ4-oxazaborine | 885700-88-9

中文名称
——
中文别名
——
英文名称
5-((4-methoxyphenyl)diazenyl)-6-methyl-2,2,6-triphenyl-3H-1,3,2λ4-oxazaborine
英文别名
——
5-((4-methoxyphenyl)diazenyl)-6-methyl-2,2,6-triphenyl-3H-1,3,2λ4-oxazaborine化学式
CAS
885700-88-9
化学式
C29H26BN3O2
mdl
——
分子量
459.355
InChiKey
UTKWATRCDKMTGV-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:
    参考文献:
    名称:
    Novel 5-(4-Substituted-phenyldiazenyl)-1,3,2λ4-oxazaborines and Their Rearrangement to 1,2,4,3λ4-Triazaborines
    摘要:
    The reaction of substituted benzenediazonium tetraphenylborates with the beta-enaminones derived from pentane-2,4-dione, 1-phenylbutane-1,3-dione, and 1,4-diphenylbutane-1,3-dione with a primary or secondary (N-methyl, N-phenyl) amino group in CH2Cl2 gives 5-(substituted-phenyldiazenyl)-2,2-diphenyl-4,6-disubstituted- 1,3,2 lambda(4)-oxazaborines or 5-(substituted-phenyldiazenyl)-2,2-diphenyl-3,4,6-trisubstituted-1,3,2 lambda(4)- oxazaborines, respectively. The reaction intermediate of these compounds has been identified, and a mechanism for the reaction has been suggested. Substituted 1,3,2 lambda(4)-oxazaborines gradually rearrange into 1,2,4,3 lambda(4)-triazaborines at temperatures above 100 degrees C.
    DOI:
    10.1021/om051078x
  • 作为产物:
    描述:
    4-amino-4-phenyl-3-buten-2-one4-Methoxybenzendiazoniumtetraphenylborat 在 sodium acetate 作用下, 以 二氯甲烷 为溶剂, 以43%的产率得到5-((4-methoxyphenyl)diazenyl)-6-methyl-2,2,6-triphenyl-3H-1,3,2λ4-oxazaborine
    参考文献:
    名称:
    Novel 5-(4-Substituted-phenyldiazenyl)-1,3,2λ4-oxazaborines and Their Rearrangement to 1,2,4,3λ4-Triazaborines
    摘要:
    The reaction of substituted benzenediazonium tetraphenylborates with the beta-enaminones derived from pentane-2,4-dione, 1-phenylbutane-1,3-dione, and 1,4-diphenylbutane-1,3-dione with a primary or secondary (N-methyl, N-phenyl) amino group in CH2Cl2 gives 5-(substituted-phenyldiazenyl)-2,2-diphenyl-4,6-disubstituted- 1,3,2 lambda(4)-oxazaborines or 5-(substituted-phenyldiazenyl)-2,2-diphenyl-3,4,6-trisubstituted-1,3,2 lambda(4)- oxazaborines, respectively. The reaction intermediate of these compounds has been identified, and a mechanism for the reaction has been suggested. Substituted 1,3,2 lambda(4)-oxazaborines gradually rearrange into 1,2,4,3 lambda(4)-triazaborines at temperatures above 100 degrees C.
    DOI:
    10.1021/om051078x
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