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1,4-bis{{6-[1,3-dihydroxy-2-(methyl)prop-2-yl]amino}-4-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)-s-triazin-2-yl}-piperazine | 1337877-30-1

中文名称
——
中文别名
——
英文名称
1,4-bis{{6-[1,3-dihydroxy-2-(methyl)prop-2-yl]amino}-4-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)-s-triazin-2-yl}-piperazine
英文别名
2-[[4-[4-[4-[(1,3-Dihydroxy-2-methylpropan-2-yl)amino]-6-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)-1,3,5-triazin-2-yl]piperazin-1-yl]-6-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)-1,3,5-triazin-2-yl]amino]-2-methylpropane-1,3-diol;2-[[4-[4-[4-[(1,3-dihydroxy-2-methylpropan-2-yl)amino]-6-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)-1,3,5-triazin-2-yl]piperazin-1-yl]-6-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)-1,3,5-triazin-2-yl]amino]-2-methylpropane-1,3-diol
1,4-bis{{6-[1,3-dihydroxy-2-(methyl)prop-2-yl]amino}-4-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)-s-triazin-2-yl}-piperazine化学式
CAS
1337877-30-1
化学式
C32H52N12O8
mdl
——
分子量
732.84
InChiKey
FLYMPTJEDLZLGH-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):
    -0.4
  • 重原子数:
    52
  • 可旋转键数:
    12
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.81
  • 拓扑面积:
    232
  • 氢给体数:
    6
  • 氢受体数:
    20

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Amino-<i>s</i>-triazines — Synthesis and stereochemistry of restricted rotational phenomena — First use of a C-2-substituted serinol in tandem with masked 4-piperidone for selective amination of cyanuric chloride
    作者:Flavia Popa、Pedro Lameiras、Eric Henon、Oana Moldovan、Agathe Martinez、Carmen Bâtiu、Yvan Ramondenc、Mircea Darabantu
    DOI:10.1139/v11-075
    日期:2011.10

    Starting from 4-piperidone monohydrate hydrochloride (or the hydrochloride of its ethylene ketal) alone, otherwise in tandem with a C-2-substituted 2-aminopropane-1,3-diol (“serinol”) as amino-nucleophiles in reaction with cyanuric chloride, the synthesis of novel N-substituted amino-s-triazines is reported. The stereochemistry of rotational phenomena occurring about the newly created C(s-triazine)–N< (exocyclic) partial double bonds in the title compounds, seen as new dendritic building blocks, is discussed.

    从4-哌啶酮单水合盐盐酸盐(或其乙烯缩醛的盐酸盐)开始,否则与C-2-取代的2-氨基丙烷-1,3-二醇(“丝氨醇”)一起,在与异氰酸氯反应中作为氨基亲核试剂,报道了新型N-取代氨基-s-三嗪的合成。讨论了在标题化合物中新建立的C(s-三嗪)-N<(外环)部分双键周围发生的旋转现象的立体化学,这被视为新的树突状构建模块。
  • Design, synthesis and structure of new dendritic melamines. First use of a tandem C-2-substituted serinol—O,O-masked 4-piperidone as a peripheral unit in iterative synthesis
    作者:Flavia Popa、Pedro Lameiras、Oana Moldovan、Maria Tomoaia-Cotisel、Eric Henon、Agathe Martinez、Carmen Sacalis、Aurora Mocanu、Yvan Ramondenc、Mircea Darabantu
    DOI:10.1016/j.tet.2012.07.096
    日期:2012.10
    The iterative chemoselective amination of cyanuric chloride to dimers of new G-2 dendritic N-substituted-2,4,6-triamino-s-triazines (melamines) having C-2-substituted 2-aminopropane-1,3-diols ('serinols') in tandem with the ethylene ketal of 4-piperidone as peripheral units is reported. The structure as a function of increasing molecular size was studied by NMR spectroscopy, DFT calculation and AFM imaging. A concise nomenclature defining the restricted rotational phenomena about the newly created C(s-triazine)-N(exocyclic) partial double bonds, seen as axes of (pro)diastereomerism, is used. We propose a new form of frontier rotamerism for the dendrimer surface, which operates over a long range. (C) 2012 Elsevier Ltd. All rights reserved.
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