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3,3-联吡嗪 | 10198-96-6

中文名称
3,3-联吡嗪
中文别名
——
英文名称
3,3'-bipyridazine
英文别名
2,2'-bipyridazine;[3,3']bipyridazinyl;3,3'-Bipyridazin;3-pyridazin-3-ylpyridazine
3,3-联吡嗪化学式
CAS
10198-96-6
化学式
C8H6N4
mdl
——
分子量
158.162
InChiKey
UXMWOEBIPQMAQT-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

  • 沸点:
    478.4±20.0 °C(Predicted)
  • 密度:
    1.239±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.5
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    51.6
  • 氢给体数:
    0
  • 氢受体数:
    4

安全信息

  • 海关编码:
    2933990090

SDS

SDS:5daf1f61006e76f7b674505f34d7327b
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反应信息

  • 作为反应物:
    描述:
    3,3-联吡嗪六羰基钨四氢呋喃 作用下, 以 四氢呋喃 为溶剂, 以34%的产率得到3,3'-联哒嗪四羰基钨(0)
    参考文献:
    名称:
    Coordination characteristics of four isomeric .alpha.-diimine ligands. .pi. Molecular orbital perturbation calculations for the bidiazines and their correlation with the properties of group 6 metal carbonyl complexes
    摘要:
    DOI:
    10.1021/ja00273a005
  • 作为产物:
    描述:
    哒嗪 在 palladium on activated charcoal 作用下, 生成 3,3-联吡嗪
    参考文献:
    名称:
    3,3'-联哒嗪配体钌配合物的共振拉曼光谱和光物理性质
    摘要:
    本报告记录了配合物 Ru(bpdz)32+ 和 [Ru(bpy)2(bpdz)]2+ 的光谱和光物理性质,其中 bpdz = 3,3'-联吡啶和 bpy = 2,2'-联吡啶. 具体来说,配合物的特点是紫外可见、发射、共振拉曼 (RR) 和瞬态共振拉曼 (TR3) 光谱数据,以及寿命测量。Ru(bpdz)32+ 配合物的 RR 光谱记录了配位配体的特征模式,而杂配配合物 [Ru(bpy)2(bpdz)]2+ 的 RR 光谱是在明智选择的激发波长下获得的,根据特定的激发波长,揭示 bpy 模式或 bpdz 模式的选择性增强,允许确定地分配观察到的电子吸收带,并将最低能量的电子跃迁确定为具有 Ru-to-bpdz 电荷转移特性。Ru(bpdz)32+ 配合物的 TR3 谱揭示了配位的 bpdz-• 阴离子自由基的特征频率...
    DOI:
    10.1021/jp0214312
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文献信息

  • [EN] PHOTOACTIVATED MOLECULES FOR LIGHT-INDUCED MODULATION OF THE ACTIVITY OF ELECTRICALLY EXCITABLE CELLS AND METHODS OF USING SAME<br/>[FR] MOLÉCULES PHOTO-ACTIVÉES POUR PHOTO-MODULATION DE L'ACTIVITÉ DE CELLULES ÉLECTRIQUEMENT EXCITABLES ET PROCÉDÉS D'UTILISATION ASSOCIÉS
    申请人:UNIV SOUTHERN CALIFORNIA
    公开号:WO2014100283A1
    公开(公告)日:2014-06-26
    Methods and compositions modulate the activity of electrically excitable cells. Photovoltaic compounds which, upon exposure to light energy, increase or decrease the electrical activity of cells. These supplement and/or replace of vision based on the conversion of light energy to electrical energy within certain cells of the visual system. A "patch" or bridge to circumvent one or more defective, damaged, or diseased cells in the visual system. Additionally, in several embodiments, subjects with normal vision can benefit from the methods, compositions, systems, and/or devices disclosed herein as normal visual acuity can be heightened. The exposure induces an energy (e.g., a receipt of light energy, conversion to electrical energy, and passage of that electrical energy) from the photovoltaic compound to the cell, thereby altering the transmembrane potential of the cell and/or the opening of one or more ion channels, thereby modulating the activity of the electrically excitable cell.
    方法和配方调节电兴奋细胞的活动。光电池化合物,在受到光能照射时,增加或减少细胞电活动。这些补充和/或替代基于将光能转化为视觉系统内某些细胞的电能的视觉。一种“贴片”或桥梁,用以绕过视觉系统中的一个或多个缺陷、损坏或病变细胞。此外,在多种实施方式中,正常视力的受试者也可以从本公开的方法、配方、系统或设备中受益,因为正常视力可以增强。照射引发能量(例如,接收光能,转化为电能,并传递该电能)从光电池化合物到细胞,从而改变细胞的跨膜电位和/或打开一个或多个离子通道,从而调节电兴奋细胞的活动。
  • [EN] PHOTOACTIVATED MOLECULES FOR LIGHT-INDUCED MODULATION OF THE ACTIVITY OF ELECTRICALLY EXCITABLE CELLS AND METHODS OF USING<br/>[FR] MOLÉCULES PHOTOACTIVÉES POUR LA MODULATION INDUITE PAR LA LUMIÈRE DE L'ACTIVITÉ DES CELLULES ÉLECTRIQUEMENT EXCITABLES ET PROCÉDÉS D'UTILISATION
    申请人:UNIV SOUTHERN CALIFORNIA
    公开号:WO2017031380A1
    公开(公告)日:2017-02-23
    Disclosed herein are methods and compositions for the modulation of the activity of electrically excitable cells. In particular, several embodiments relate to the use of photovoltaic compounds which, upon exposure to light energy, increase or decrease the electrical activity of cells.
    公开了用于调节电兴奋性细胞活动的方法和组合物。特别是,几个实施例涉及使用光伏化合物,该化合物在暴露于光能时增加或减少细胞的电活动。
  • Synthesis, electrochemistry and emission spectroscopy in fluid solution of four isomeric (α-diimine)Re(CO)3Hal complexes
    作者:Wolfgang Kaim、Horst E.A. Kramer、Conny Vogler、Jochen Rieker
    DOI:10.1016/0022-328x(89)87212-2
    日期:1989.5
    Complexes (bdz)Re(CO)3Hal (Hal = Cl or Br) derived from the four isomeric bidiazine (bdz) chelate ligands 3,3′-bipyridazine, 2,2′-bipyrazine, 2,2′- and 4,4′-bipyrimidine have been synthesized from Re(CO)5Hal by thermal substitution. All the complexes were found to show long-wavelength emission at room temperature in chloroform solution after irradiation into the metal-to-ligand charge transfer (MLCT)
    衍生自四个异构二氮杂(bdz)螯合配体3,3'-联哒嗪,2,2'-联吡嗪,2,2'-和4的配合物(bdz)Re(CO)3 Hal(Hal = Cl或Br)通过热取代从Re(CO)5 Hal合成了4'-联嘧啶。发现所有配合物在辐照到金属-配体电荷转移(MLCT)谱带后,在氯仿溶液中均在室温下显示出长波发射。光谱数据和电化学还原电位证实了中性Re(CO)3 Hal片段对α-二亚胺π系统具有优异的极化能力,并且电化学和光物理数据可以与游离配体,其阴离子自由基,和其他d 6金属(W 0,Ru II)配合物。
  • Alkyne derivatives as tracers for metabotropic glutamate receptor binding
    申请人:Cosford Peter Nicholas David
    公开号:US20070060618A1
    公开(公告)日:2007-03-15
    The present invention is directed to isotopically labeled alkyne derivative compounds, particularly 11 C, 13 C, 14 C, 18 F, 15 O, 13 N, 35 S, 2 H, and 3 H labeled compounds. In particular, the present invention is directed to 11 C, 13 C, 14 C, 18 F, 15 O, 13 N, 35 S, 2 H, and 3 H labeled heterocyclic alkynes and methods of their preparation. The present invention further includes a method of use of the 11 C, 18 F, 15 O, or 13 N labeled heterocyclic alkyne compounds as tracers in positron emission tomography (PET) imaging, particularly in the study of metabolic conditions in mammals, specifically conditions modulated by metabotropic glutamate receptors subtype 5 (mGluR5).
    本发明涉及同位素标记的炔基衍生物化合物,特别是11C、13C、14C、18F、15O、13N、35S、2H和3H标记的化合物。具体而言,本发明涉及11C、13C、14C、18F、15O、13N、35S、2H和3H标记的杂环炔烃及其制备方法。本发明还包括将11C、18F、15O或13N标记的杂环炔烃化合物用作正电子发射断层扫描(PET)成像中的示踪剂的使用方法,特别是在哺乳动物代谢状况的研究中,特别是通过代谢型谷氨酸受体亚型5(mGluR5)调节的状况。
  • Pyridazine and Pyrrole Compounds, Processes For Obtaining Them and Uses
    申请人:Dubreuil Didier Max
    公开号:US20100298562A1
    公开(公告)日:2010-11-25
    The present invention relates to nonlinear oligopyridazine compounds, to processes for obtaining them, to their uses, and also to their reduction to oligopyrroles and to the uses of the pyridazinylpyrrole and oligopyrrole compounds obtained. The invention relates in particular to the uses as medicaments, in particular for treating pathologies such as cancer, bacterial infections or parasitic infections, and also the uses in the materials, environmental, electronics and optics field.
    本发明涉及非线性寡吡啶化合物,以及获得它们的方法,它们的用途,以及将它们还原为寡吡咯和所获得的吡啶基吡咯和寡吡咯化合物的用途。该发明特别涉及用作药物的用途,特别是用于治疗癌症、细菌感染或寄生虫感染等病理的用途,以及在材料、环境、电子和光学领域的用途。
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