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4,4'-(6,6'-(propane-2,2-diyl)bis(2H-benzo-[e][1,3]oxazine-6,3(4H)-diyl))dianiline | 1217504-94-3

中文名称
——
中文别名
——
英文名称
4,4'-(6,6'-(propane-2,2-diyl)bis(2H-benzo-[e][1,3]oxazine-6,3(4H)-diyl))dianiline
英文别名
4-[6-[2-[3-(4-Aminophenyl)-2,4-dihydro-1,3-benzoxazin-6-yl]propan-2-yl]-2,4-dihydro-1,3-benzoxazin-3-yl]aniline;4-[6-[2-[3-(4-aminophenyl)-2,4-dihydro-1,3-benzoxazin-6-yl]propan-2-yl]-2,4-dihydro-1,3-benzoxazin-3-yl]aniline
4,4'-(6,6'-(propane-2,2-diyl)bis(2H-benzo-[e][1,3]oxazine-6,3(4H)-diyl))dianiline化学式
CAS
1217504-94-3
化学式
C31H32N4O2
mdl
——
分子量
492.621
InChiKey
PHTULNZADPYZPX-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):
    6.3
  • 重原子数:
    37
  • 可旋转键数:
    4
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    77
  • 氢给体数:
    2
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    2,2'-(4,4'-(6,6'-(propane-2,2-diyl)bis(2H-benzo[e][1,3]oxazine-6,3(4H)-diyl))bis(4,1-phenylene))bis(4,5,6,7-tetrachloroisoindoline-1,3-dione)一水合肼 作用下, 以 乙醚 为溶剂, 反应 5.0h, 以90%的产率得到4,4'-(6,6'-(propane-2,2-diyl)bis(2H-benzo-[e][1,3]oxazine-6,3(4H)-diyl))dianiline
    参考文献:
    名称:
    Primary Amine-Functional Benzoxazine Monomers and Their Use for Amide-Containing Monomeric Benzoxazines
    摘要:
    Amino-functional benzoxazine monomers have been successfully prepared. Several routes have been applied to incorporate amino group into benzoxazine structure. These approaches include reduction of the corresponding nitro-functional benzoxazines and deprotection of protected amino-functional benzoxazine monomers. Various approaches that allow primary amine groups to be prepared without damaging the existing benzoxazine groups have been evaluated. Tetrachlorophthalimide and trifluoroacetyl are found to be suitable protecting groups. In addition, a model compound of amide-functional benzoxazines is prepared from primary amine-functional benzoxazine. Fourier transform infrared spectroscopy (FTIR) and H-1 and C-13 nuclear magnetic resonance spectroscopy (NMR) are used to characterize the structure of the monomers. The polymerization behavior of amino-functional monomers and model compound are studied by differential scanning calorimetry (DSC).
    DOI:
    10.1021/ma902556k
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