aniline benzenesulfonate | 4484-20-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: aniline benzenesulfonate
• 英文别名: Anilinyl benzenesulfonate；Benzenesulfonate;phenylazanium；benzenesulfonate;phenylazanium
• CAS: 4484-20-2
• 化学式: C₆H₆O₃S*C₆H₇N
• 分子量: 251.306
• InChiKey: NGYOVXUBIWJNIU-UHFFFAOYSA-N

物化性质

• 熔点：
  231 °C(Solv: ethanol (64-17-5); water (7732-18-5))

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  17
• 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：
  88.8
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  癸腈 、 aniline benzenesulfonate 生成 N-phenyl-decanamidine
  参考文献：
  名称：

  Charlton et al., Journal of the Chemical Society, 1951, p. 485,489, 492

  摘要：

  DOI：
• 作为产物：
  描述：

  N-亚磺酰苯胺 在 乙醚 作用下， 生成 aniline benzenesulfonate
  参考文献：
  名称：

  Gilman; Morris, Journal of the American Chemical Society, 1926, vol. 48, p. 2403

  摘要：

  DOI：
• 作为试剂：
  描述：

  2-氰基吡啶 在 aniline benzenesulfonate 作用下， 生成 吡啶-2-羧酰胺
  参考文献：
  名称：

  Manufacture of amidines

  摘要：

  公开号：

  US02451779A1

文献信息

• Nucleophilic substitution reactions of indan-2-yl arenesuifonates with anilines in methanol
  作者：Ikchoon Lee、Young Sook Lee、Chul Huh、Hai Whang Lee、Byung Choon Lee

  DOI：10.1039/p29930002415

  日期：——

  The nucleophilic substitution reactions of (Y)-indan-2-yl (Z)-arenesulfonates with (X)-anilines in methanol at 55.0 °C are reported. Sign reversals in all three second-order cross-interaction constants, ρxy, ρyz and ρxz, are observed at non-interaction points z=–0.11 (ρxy= 0), x=–0.02 (ρyz= 0) and Y= 0.43 (ρxz= 0) respectively, which have been ascribed to an unusually large third-order cross-interaction

  报道了在55.0°C下，（Y）-茚满-2-基（Z）-芳烃磺酸盐与（X）-苯胺在甲醇中的亲核取代反应。符号颠倒在所有三个第二阶交叉相互作用常数，ρ XY，ρ YZ和ρ XZ，在非交互点观察ž = -0.11（ρ XY = 0），X = -0.02（ρ YZ = 0）和ÿ = 0.43（ρ XZ = 0）分别，已被归因于异常大的第三阶交叉相互作用常数，ρ XYZ = -0.53，反应系列。一个S Ñ具有倾斜，平行2过渡状态层积并在亲核试剂（X），底物（Y）和离去基团（Z）位移的三个苯环的结构，提出的合理化强三体由大的耦合表现ρ XYZ价值。
• Charge control agent, toner, image forming method, and image forming apparatus
  申请人：Yano Tetsuya

  公开号：US20090202927A1

  公开（公告）日：2009-08-13

  To provide: a charge control agent having negative chargeability, which contributes to environmental conservation and the like to an increased degree, has high performance (high charge amount, quick rise-up of charge, excellent stability with time, and high environmental stability), and has improved dispersibility; a toner for developing an electrostatic charge image containing the charge control agent; and an image forming method and an image forming apparatus each using the toner for developing an electrostatic charge image. A charge control agent for controlling a charged state of powder, characterized by including one or more units each represented by the following chemical formula (1) in a molecule.

  提供：一种具有负电荷性能的充电控制剂，可更有效地促进环境保护等，具有高性能（高电荷量，快速电荷上升，优异的时间稳定性和高环境稳定性），并具有改善的分散性；一种包含充电控制剂的用于开发静电充电图像的色调剂；以及使用用于开发静电充电图像的色调剂的图像形成方法和图像形成设备。一种用于控制粉末的带电状态的充电控制剂，其特征在于分子中包含由以下化学式（1）表示的一个或多个单元。
• Charge control agent, toner, image forming method and image forming apparatus
  申请人：Canon Kabushiki Kaisha

  公开号：EP2184645A2

  公开（公告）日：2010-05-12

  A charge control agent for controlling a charged state of powder contains a polymer having a unit having a structure represented by the chemical formula (19): wherein R represents -A25-SO2R25. R25w, R25x, and R25y are selected from combinations described in the following items (i) and (ii). For the item (i), A25 and R25 are selected from combinations described in the following items (i-A) and (i-B); for the item (ii), A25 and R25 are selected from combinations described in the following item (ii-A): (i) R25w and R25x each represent a hydrogen atom, and R25y represents a CH3 group or a hydrogen atom; (i-A) A25 represents a substituted or unsubstituted aliphatic hydrocarbon structure; R25 represents a halogen atom or OR25a where R25a represents a substituted or unsubstituted aliphatic hydrocarbon structure, a substituted or unsubstituted aromatic ring structure, or a substituted or unsubstituted heterocyclic structure; (i-B) A25 represents a substituted or unsubstituted aromatic ring structure, or a substituted or unsubstituted heterocyclic structure; R25 represents OH, a halogen atom, ONa, OK, or OR25a where R25a represents a substituted or unsubstituted aliphatic hydrocarbon structure, a substituted or unsubstituted aromatic ring structure, or a substituted or unsubstituted heterocyclic structure; (ii) R25w and R25X each independently represent a halogen atom or a hydrogen atom; R25y represents a CH3 group, a halogen atom, or a hydrogen atom; at least one of R25w, R25X, and R25y represents a halogen atom; (ii-A) A25 represents a substituted or unsubstituted aliphatic hydrocarbon structure, a substituted or unsubstituted aromatic ring structure, or a substituted or unsubstituted heterocyclic structure; R25 represents OH, a halogen atom, ONa, OK, or OR25a where R25a represents a substituted or unsubstituted aliphatic hydrocarbon structure, a substituted or unsubstituted aromatic ring structure, or a substituted or unsubstituted heterocyclic structure.

  一种用于控制粉末带电状态的电荷控制剂含有一种聚合物，该聚合物具有化学式（19）表示的结构单元： 其中 R 代表-A25-SO2R25。R25w、R25x和R25y选自以下第(i)和(ii)项所述的组合。 对于第(i)项，A25 和 R25 选自以下第(i-A)和(i-B)项所述的组合；对于第(ii)项，A25 和 R25 选自以下第(ii-A)项所述的组合： (i) R25w 和 R25x 各代表一个氢原子，R25y 代表一个 CH3 基团或一个氢原子； (i-A) A25 代表取代或未取代的脂族烃结构；R25 代表卤素原子或 OR25a，其中 R25a 代表取代或未取代的脂族烃结构、取代或未取代的芳环结构或取代或未取代的杂环结构； (i-B) A25 代表取代或未取代的芳环结构，或取代或未取代的杂环结构； R25 代表 OH、卤素原子、ONa、OK 或 OR25a，其中 R25a 代表取代或未取代的脂族 烃结构、取代或未取代的芳环结构，或取代或未取代的杂环结构； (ii) R25w 和 R25X 各自独立地代表卤素原子或氢原子；R25y 代表 CH3 基团、卤素原子或氢原子；R25w、R25X 和 R25y 中至少有一个代表卤素原子； (iii-A) A25 代表取代或未取代的脂族烃结构、取代或未取代的芳环结构或取代或未取代的杂环结构； R25 代表 OH、卤素原子、ONa、OK 或 OR25a，其中 R25a 代表取代或未取代的脂族烃结构、取代或未取代的芳环结构或取代或未取代的杂环结构。
• Partridge, Journal of Pharmacy and Pharmacology, 1952, vol. 4, p. 533
  作者：Partridge

  DOI：——

  日期：——
• Effect of theory-based feature correlations on typicality judgments
  作者：Woo-Kyoung Ahn、Jessecae K. Marsh、Christian C. Luhmann、Kevin Lee

  DOI：10.3758/bf03195270

  日期：2002.1

  In the present study, we examine what types of feature correlations are salient in our conceptual representations. It was hypothesized that of all possible feature pairs, those that are explicitly recognized as correlated (i.e., explicit pairs) and affect typicality judgments are the ones that are more likely theory based than are those that are not explicitly recognized (i.e., implicit pairs). Real-world categories and their properties, taken from Malt and Smith (1984), were examined. We found that explicit pairs had a greater number of asymmetric dependency relations (i.e., one feature depends on the other feature, but not vice versa) and stronger dependency relations than did implicit pairs, which were statistically correlated in the environment but were not recognized as such. In addition, people more often provided specific relation labels for explicit pairs than for implicit pairs; these labels were most often causal relations. Finally, typicality judgments were more affected when explicit correlations were broken than when implicit correlations were broken. It is concluded that in natural categories, feature correlations that are explicitly represented and affect typicality judgments are the ones about which people have theories.