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2,5-diamino-[1,4]dithiobenzoquinone | 108119-79-5

分子结构分类

中文名称
——
中文别名
——
英文名称
2,5-diamino-[1,4]dithiobenzoquinone
英文别名
2.5-Diamino-dithio-p-chinon;2,5-Diamino-[1,4]dithiobenzochinon;2,5-Diaminocyclohexa-2,5-diene-1,4-dithione
2,5-diamino-[1,4]dithiobenzoquinone化学式
CAS
108119-79-5
化学式
C6H6N2S2
mdl
——
分子量
170.259
InChiKey
HCQMESOFNXNWTD-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):
    0.3
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    116
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    alkaline earth salt of/the/ methylsulfuric acid 在 硫酸 作用下, 生成 2,5-diamino-[1,4]dithiobenzoquinone
    参考文献:
    名称:
    Green; Perkin, Journal of the Chemical Society, 1903, vol. 83, p. 1205
    摘要:
    DOI:
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文献信息

  • Phosphate salts of monomers for PBZ and their use in preparing PBZ polymers
    申请人:THE DOW CHEMICAL COMPANY
    公开号:EP0393559A2
    公开(公告)日:1990-10-24
    PBZ polymers are synthesized by the reaction of AA- and BB-monomers. The BB-monomer is conveniently synthesized and isolated as a phosphate salt having a uniform number of phosphate ions associated with each BB-monomer ion. Such high purity monophosphate and diphosphate salts can be obtained by precipitating the monomer from an aqueous acid solution by adjusting the pH balance or from a mixture of phosphoric acid and a volatile, polar, saturated organic liquid at a rela­tively low temperature.
    PBZ 聚合物是通过 AA 和 BB 单体反应合成的。BB 单体可方便地合成和分离为磷酸盐,这种磷酸盐具有与每个 BB 单体离子相关联的均匀数量的磷酸根离子。这种高纯度的单磷酸盐和二磷酸盐可通过调节 pH 值平衡从酸性溶液中沉淀单体,或在相对较低的温度下从磷酸和挥发性、极性、饱和有机液体的混合物中沉淀单体而获得。
  • Polybenzazole polymers containing perfluorocyclobutane rings
    申请人:THE DOW CHEMICAL COMPANY
    公开号:EP0476560A1
    公开(公告)日:1992-03-25
    Polybenzazole polymers may contain perfluorocyclobutane rings to provide a flexible moiety which is stable at high temperatures.
    苯唑聚合物可能含有全氟环丁烷环,以提供在高温下稳定的柔性分子。
  • Staged polymerization of polybenzazole polymers
    申请人:THE DOW CHEMICAL COMPANY
    公开号:EP0481402A2
    公开(公告)日:1992-04-22
    It is advantageous to prepare oligomers of polybenzazole polymers by reaction of AA-PBZ monomer with an excess of BB-PBZ monomer. The resulting oligomer dopes may be stored at a temperature at which they remain pumpable until such time as the dope can be advanced to higher molecular weight by adding additional AA-PBZ monomer. The molecular weight of the polymer may be adjusted by controlling the amount of chain extender and/or chain terminator added to oligomer mixtures as they are advanced to final molecular weight.
    通过 AA-PBZ 单体与过量的 BB-PBZ 单体反应制备聚苯唑聚合物的低聚物是非常有利的。得到的低聚物掺合料可以储存在一定的温度下,在加入额外的 AA-PBZ 单体使掺合料达到更高的分子量之前,它们仍然是可泵送的。聚合物的分子量可以通过控制添加到低聚物混合物中的扩链剂和/或链终止剂的量来调整,因为它们会被提升到最终分子量。
  • Process to improve adhesion of pbo and pbt fibers in a matrix resin
    申请人:THE DOW CHEMICAL COMPANY
    公开号:EP0500046A2
    公开(公告)日:1992-08-26
    A method for sulfonating fibers or films comprising polybenzazole polymers is described. These sulfonated polybenzazole fibers are incorporated into composites containing a matrix resin such as an epoxy resin. The interfacial shear strength of these sulfonated polybenzazole fiber-containing composites is significantly improved over the interfacial shear strength of similar composites containing unsulfonated polybenzazole fibers.
    本文介绍了一种磺化聚苯唑聚合物纤维或薄膜的方法。将这些磺化聚苯唑纤维加入含有基体树脂(如环氧树脂)的复合材料中。与含有未磺化聚苯唑纤维的类似复合材料的界面剪切强度相比,这些含有磺化聚苯唑纤维的复合材料的界面剪切强度有显著提高。
  • Preparation of poly(benz(ox, imid, thi)azole) polymers
    申请人:EASTMAN KODAK COMPANY
    公开号:EP0522469A2
    公开(公告)日:1993-01-13
    A method for the preparation of poly(benzoxazole)s, poly(benzimidazole)s, and poly(benzthiazole)s. In the presence of solvent and catalyst, reacting carbon monoxide, an aromatic halide reactant having the general formula X¹-Ar¹-Z¹ and an aromatic amine reactant having the general formula Z²-Ar²-M¹, wherein X¹ and Z¹ are non-ortho, Z² and M¹ are non-ortho, one of Z¹ and Z² is X² and the other one is M², -Ar¹- and -Ar²- are each independently selected from the group consisting of aromatic and hetero-aromatic moieties having a total of ring carbons and heteroatoms of from 6 to 20, X¹ and X² are each independently selected from the group consisting of -I and -Br, and M¹ and M² are each independently selected from moieties having an -NH₂ radical and, ortho to the -NH₂ radical, a radical selected from the group consisting of -NH₂, -OH, and -SH.
    一种制备聚(苯并恶唑)、聚(苯并咪唑)和聚(苯并噻唑)的方法。在溶剂和催化剂存在下,使一氧化碳、通式为 X¹-Ar¹-Z¹ 的芳族卤化物反应物和通式为 Z²-Ar²-M¹ 的芳族胺反应物反应,其中 X¹ 和 Z¹ 为非正交,Z² 和 M¹ 为非正交,Z¹ 和 Z² 中的一个为 X²,另一个为 M²、-Ar¹-和-Ar²-各自独立地选自由环碳原子和杂原子总数为 6 至 20 的芳香族和杂芳香族分子组成的组,X¹和 X² 各自独立地选自由-I 和-Br 组成的组,M¹和 M² 各自独立地选自由具有-NH₂基的分子以及与-NH₂基正交的选自由-NH₂、-OH 和-SH 组成的组的基。
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