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1,4-bis(2,3-dihydro-1H-perimidin-2-yl)benzene | 73858-20-5

中文名称
——
中文别名
——
英文名称
1,4-bis(2,3-dihydro-1H-perimidin-2-yl)benzene
英文别名
1,4-bis(2,3-dihydro-2-perimidinyl)benzene;2-[4-(2,3-dihydro-1H-perimidin-2-yl)phenyl]-2,3-dihydro-1H-perimidine
1,4-bis(2,3-dihydro-1H-perimidin-2-yl)benzene化学式
CAS
73858-20-5
化学式
C28H22N4
mdl
——
分子量
414.509
InChiKey
UIPCVJKRSFIVPJ-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

物化性质

  • 熔点:
    222-224 °C(Solv: ethanol (64-17-5))
  • 沸点:
    776.4±60.0 °C(Predicted)
  • 密度:
    1.262±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    7.2
  • 重原子数:
    32
  • 可旋转键数:
    2
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    48.1
  • 氢给体数:
    4
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    1,4-bis(2,3-dihydro-1H-perimidin-2-yl)benzene 在 sulfur 作用下, 以92%的产率得到bis-1,4-(1H-perimidin-2-yl)benzene
    参考文献:
    名称:
    二烯的杂环类似物
    摘要:
    DOI:
    10.1007/bf00475399
  • 作为产物:
    描述:
    对苯二甲醛1,8-二氨基萘 反应 0.08h, 以79%的产率得到1,4-bis(2,3-dihydro-1H-perimidin-2-yl)benzene
    参考文献:
    名称:
    一种新颖的无催化剂机械化学方案,用于合成2,3-二氢-1H-嘧啶
    摘要:
    已经开发了一种快速,高效且绿色的研磨辅助方法,用于合成2,3-二氢-1 H-亚氨基吡啶。用研钵和研杵将1,8-二氨基萘和醛研磨5分钟,使产品收率适中至优异。该方法最大限度地减少了传统的后处理和柱色谱技术的使用。
    DOI:
    10.1002/jhet.3880
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文献信息

  • A novel catalyst-free, eco-friendly, on water protocol for the synthesis of 2,3-dihydro-1H-perimidines
    作者:Nissy Ann Harry、Reeba Mary Cherian、S. Radhika、Gopinathan Anilkumar
    DOI:10.1016/j.tetlet.2019.150946
    日期:2019.8
    The first greenest methodology for the synthesis of 2,3-dihydro-1H-perimidines on water is described. 1,8-Diamino naphthalene was reacted with different types of aldehydes at room temperature to furnish the product in moderate to excellent yields in 30 min. A multi-gram scale reaction is also performed to ensure the scalability of the reaction.
    描述了在上合成2,3-二氢-1 H-亚氨基吡啶的第一种最绿色的方法。使1,8-二氨基萘与不同类型的醛在室温下反应,以在30分钟内以中等至极好的收率提供该产品。还进行了克级反应,以确保反应的可扩展性。
  • (Triazinediyl)bis sulfamic acid-functionalized silica-coated magnetite nanoparticles: Preparation, characterization and application as an efficient catalyst for synthesis of mono-, bis-, tris- and spiro-perimidines
    作者:Mohammad Ali Bodaghifard、Sajad Asadbegi、Zahra Bahrami
    DOI:10.1007/s13738-016-0985-9
    日期:2017.2
    (Triazinediyl)bis sulfamic acid-functionalized silica-coated magnetite nanoparticles have been prepared and applicated as an efficient catalyst for synthesis of mono-, bis-, tris- and spiro-perimidines. The desired products have been synthesized in high purity and good yields. The workup procedure of reaction is simple. The catalyst was easily separated from the reaction mixture with the assistance
    已经制备了(三嗪二基)双氨基磺酸官能化的二氧化硅涂覆的磁矿纳米颗粒,并将其用作合成单,双,三和螺过的嘧啶的有效催化剂。所需的产物已经以高纯度和高收率合成。反应的后处理步骤很简单。在外部磁场的帮助下,容易将催化剂从反应混合物中分离出来,并重复使用几次,而不会降低催化活性。通过透射电子显微镜,扫描电子显微镜,粉末X射线衍射,能量分散光谱仪,傅立叶变换红外光谱仪和振动样品磁强计来表征核/壳纳米颗粒。
  • Application of a New Bifunctional Nanocatalyst Mn/SO <sub>3</sub> H@zeolite-Y in Rapid Synthesis of 2-Aryl Mono- and <i>bis</i> -Perimidines
    作者:Mehdi Kalhor、Raheleh Gaeini、Bahar Molaei
    DOI:10.1080/00304948.2023.2186652
    日期:2023.11.2
    Published in Organic Preparations and Procedures International: The New Journal for Organic Synthesis (Vol. 55, No. 6, 2023)
    发表于《国际有机制备和程序:有机合成新杂志》(第 55 卷,第 6 期,2023 年)
  • STARSHIKOV N. M.; POZHARSKIJ A., XIMIYA GETEROTSIKL. SOEDIN., 1980, HO 1, 96-100
    作者:STARSHIKOV N. M.、 POZHARSKIJ A.
    DOI:——
    日期:——
  • Compositions and Methods Related to Fructosamine-3-Kinase Inhibitors
    申请人:Schwartz Michael
    公开号:US20100297046A1
    公开(公告)日:2010-11-25
    The invention relates to compounds and methods for inhibiting production and function of 3-deoxyglucosone and other alpha-dicarbonyl sugars in skin, by way of fructosamine-3-kinase inhibition, thereby treating or prevention various diseases, disorders or conditions. Additionally, the invention relates to treatment of various diseases, disorders or conditions associated with or mediated by oxidative stress since 3DG induces ROS and AGEs, which are associated with the inflammatory response caused by oxidative stress.
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