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tert-butyl N-[3-[[4-[4-[4,6-bis[4-[4-[bis[3-[(2-methylpropan-2-yl)oxycarbonylamino]propyl]amino]-6-piperidin-1-yl-1,3,5-triazin-2-yl]piperazin-1-yl]-1,3,5-triazin-2-yl]piperazin-1-yl]-6-piperidin-1-yl-1,3,5-triazin-2-yl]-[3-[(2-methylpropan-2-yl)oxycarbonylamino]propyl]amino]propyl]carbamate | 1016650-76-2

中文名称
——
中文别名
——
英文名称
tert-butyl N-[3-[[4-[4-[4,6-bis[4-[4-[bis[3-[(2-methylpropan-2-yl)oxycarbonylamino]propyl]amino]-6-piperidin-1-yl-1,3,5-triazin-2-yl]piperazin-1-yl]-1,3,5-triazin-2-yl]piperazin-1-yl]-6-piperidin-1-yl-1,3,5-triazin-2-yl]-[3-[(2-methylpropan-2-yl)oxycarbonylamino]propyl]amino]propyl]carbamate
英文别名
——
tert-butyl N-[3-[[4-[4-[4,6-bis[4-[4-[bis[3-[(2-methylpropan-2-yl)oxycarbonylamino]propyl]amino]-6-piperidin-1-yl-1,3,5-triazin-2-yl]piperazin-1-yl]-1,3,5-triazin-2-yl]piperazin-1-yl]-6-piperidin-1-yl-1,3,5-triazin-2-yl]-[3-[(2-methylpropan-2-yl)oxycarbonylamino]propyl]amino]propyl]carbamate化学式
CAS
1016650-76-2
化学式
C87H150N30O12
mdl
——
分子量
1808.34
InChiKey
BAVBJAYQWFKUTI-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):
    12.9
  • 重原子数:
    129
  • 可旋转键数:
    48
  • 环数:
    10.0
  • sp3杂化的碳原子比例:
    0.79
  • 拓扑面积:
    424
  • 氢给体数:
    6
  • 氢受体数:
    36

反应信息

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文献信息

  • Kilogram-Scale Synthesis of a Second-Generation Dendrimer Based on 1,3,5-Triazine Using Green and Industrially Compatible Methods with a Single Chromatographic Step
    作者:Abdellatif Chouai、Eric E. Simanek
    DOI:10.1021/jo702462t
    日期:2008.3.1
    A kilogram scale, divergent and iterative synthesis of a second generation, triazine dendrimer with 12 protected amines on the periphery using common laboratory equipment is reported. The route benefits from common reaction conditions, inexpensive reagents, and aqueous solvents. From the monomers, the desired product dendrimer-the last uncommitted intermediate that leads to a range of committed, generation three targets-can be obtained in 70% overall yield. Of critical importance in the execution of this divergent synthesis is the differential reactivity of chlorine atoms of trichlorotriazine. The stepwise, nucleophilic aromatic substitution of these atoms with amine nucleophiles is both the basis for the dendrimer growth as well as incorporation of solubilizing piperidine groups. Intermediates are obtained and purified through precipitation and/or extraction protocols with the exception of the final product. Isolation of the target dendrimer requires a single silica gel plug filtration. The purity of this material is assessed at >93%, a level consistent with and/or exceeding other commercially available targets.
  • Large Scale, Green Synthesis of a Generation-1 Melamine (Triazine) Dendrimer
    作者:Abdellatif Chouai、Vincent J. Venditto、Eric E. Simanek
    DOI:10.1002/0471264229.os086.16
    日期:2009.12.18
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