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四氯琥珀酸 | 3875-85-2

中文名称
四氯琥珀酸
中文别名
——
英文名称
Tetrachlor-bernsteinsaeure
英文别名
tetrachlorosuccinic acid;2,2,3,3-Tetrachlorobutanedioic acid
四氯琥珀酸化学式
CAS
3875-85-2
化学式
C4H2Cl4O4
mdl
——
分子量
255.869
InChiKey
LIZCTYVUVWUZMN-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:
    188-190 °C
  • 沸点:
    197.5±35.0 °C(Predicted)
  • 密度:
    1.976±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.7
  • 重原子数:
    12
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    74.6
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    四氯琥珀酸 为溶剂, 生成 三氯丙烯酸二氧化碳
    参考文献:
    名称:
    Mertens, Ralf; Sonntag, Clemens von, Journal of the Chemical Society. Perkin transactions II, 1994, # 10, p. 2181 - 2186
    摘要:
    DOI:
  • 作为产物:
    描述:
    Tetrachlorbernsteinsaeure-dichlorid 在 作用下, 生成 四氯琥珀酸
    参考文献:
    名称:
    Kaupp,J. et al., Justus Liebigs Annalen der Chemie, 1964, vol. 677, p. 71 - 77
    摘要:
    DOI:
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文献信息

  • Process for producing diphenylmethane dicarbamates
    申请人:Asahi Kasei Kogyo Kabushiki Kaisha
    公开号:EP0110732A2
    公开(公告)日:1984-06-13
    A process for producing a diphenylmethane dicarbamate by reacting a N-phenylcarbamate with a methylenating agent is disclosed. The process is carried out by condensing N-phenylcarbamate in two steps using a combination of two different types of acid catalysts. The catalysts exhibit a strong catalizing effect and yet can be radily separated from the reaction mixture. The process produces dineuclear diphenylmethane dicarbamates in high selectivity. The acid catalysts can be easily recovered from the reaction mixtures and put to another use.
    本发明公开了一种通过 N-苯基氨基甲酸酯与甲烯化剂反应生产二苯基甲烷二氨基甲酸酯的工艺。该工艺使用两种不同类型的酸催化剂,分两步缩合 N-苯基氨基甲酸酯。催化剂具有很强的催化作用,而且可以从反应混合物中快速分离出来。该工艺能以高选择性生产二核二苯基甲烷二氨基甲酸酯。酸催化剂可以很容易地从反应混合物中回收,并用于其他用途。
  • Method for manufacture of diphenylmethane diisocyanates
    申请人:Asahi Kasei Kogyo Kabushiki Kaisha
    公开号:EP0123412A1
    公开(公告)日:1984-10-31
    Manufacture of a diphenylmethane diisocyanate for an N-phenylcarbamate is economically accomplished in high yield with high selectivity by a method which comprises (A) a process of methylenation forthe formation of a condensation product containing at least 80 mol% of a dinuclear diphenylmethane dicarbamate by the steps of 1) causing a methylenating agent to react upon at least 2 moles of an N-phenylcarbamate, based on 1 mole of the methylene group of said methylenating agent, in a liquid phase in the presence of an aqueous inorganic acid solution, 2) separating the resultant reaction mixture into the aqueous inorganic acid solution and an organic phase reaction mixture containing substantially none of said inorganic acid, and 3) subsequently treating said organic phase reaction mixture in the presence of an N-phenylcarbamate and a carboxylic acid having a pKa of not more than 4 in an aqueous solution at a temperature of25°C or a solid acid or an acid consisting of said two acids thereby converting a reaction intermediate possessing a methylene-amino bond and contained in said organic phase reaction mixture to a diphenylmethane dicarbamate, and (B) a process of thermal decomposition by the steps of allowing a mixture comprising 1 to 50% by weight of the condensation product obtained in said process of (A) and 99 to 50% by weight of a thermal decomposition solvent having a boiling point under atmospheric pressure in the range of 120 to 350%C and being inactive to isocyanates to flow down into a reactor maintained attemperatu res in the range of 180 to 380°C through the upper part thereof, causing said mixture to come into counterflow contact with a carrier introduced into said reactor upwardly via the lower part thereof thereby producing an organic hydroxyl compound, allowing said organic hydroxyl compound to be discharged from said reactor in the form of vapor in conjunction with said carrier through the upper part thereof, and withdrawing the resultant isocyanate solution from said reactor through the lower part thereof.
    用 N-苯基氨基甲酸酯制造二苯基甲烷二异氰酸酯是一种高产率和高选择性的经济 方法,该方法包括 (A) 通过以下步骤形成含有至少 80 摩尔二核二苯基甲烷二氨基甲酸酯的缩合产物的亚 甲基化过程:1) 使亚甲基化剂与至少 2 摩尔的 N-苯基氨基甲酸酯反应、1) 在无机酸水溶液存在下,使亚甲基化剂在液相中与至少 2 摩尔的 N-苯基氨基甲酸酯发生反应,以所述亚甲基化剂的 1 摩尔亚甲基为基准、2) 将生成的反应混合物分离为无机酸水溶液和基本上不含所述无机酸的有机相反应混合物、3) 随后在温度为 25°C 的水溶液中,在 N-苯基氨基甲酸酯和 pKa 不大于 4 的羧酸或固体酸或由上述两种酸组成的酸的存在下处理上述有机相反应混合物,从而将上述有机相反应混合物中含有的具有亚甲基氨基键的反应中间体转化为二苯基甲烷二氨基甲酸酯、(B) 热分解工艺,其步骤为:使包含 1 至 50%(按重量计)在所述(A)工艺中获得的缩合产物和 99 至 50%(按重量计)的热分解溶剂的混合物流下,该溶剂在大气压下的沸点在 120 至 350℃之间,对异氰酸酯不活泼,并通过其上部流入温度保持在 180 至 380℃之间的反应器中、使所述混合物与通过其下部向上进入所述反应器的载体逆流接触,从而产生有机羟基化合物,使所述有机羟基化合物与所述载体一起通过其上部以蒸汽的形式排出所述反应器,并通过其下部将由此产生的异氰酸酯溶液从所述反应器中抽出。
  • Andrographolide derivatives to treat viral infections
    申请人:Liu Hai Rui
    公开号:US20060223785A1
    公开(公告)日:2006-10-05
    The present invention provides a methods and compositions for treating a host afflicted with a viral infection, particularly a Flaviviridae infection, including hepatitis C infection, comprising administering an effective antiviral amount of a derivative of andrographolide alone or in combination or alternation with another antiviral compound.
    本发明提供了一种治疗病毒感染宿主的方法和组合物,特别是病毒科感染,包括丙型肝炎感染,包括单独或与另一种抗病毒化合物联合或交替使用有效抗病毒量的穿心莲内酯衍生物。
  • Processes for producing dibasic acids and derivatives of dibasic acids
    申请人:LILLY CO ELI
    公开号:US02426224A1
    公开(公告)日:1947-08-26
  • Doughty; Freeman, Journal of the American Chemical Society, 1922, vol. 44, p. 639
    作者:Doughty、Freeman
    DOI:——
    日期:——
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