六氢-1,3,5-三(4-甲基苯基)-1,3,5-三嗪 | 6639-47-0

• 分子结构分类: 有机化合物 - 有机氮化合物
• 中文名称: 六氢-1,3,5-三(4-甲基苯基)-1,3,5-三嗪
• 英文名称: 1,3,5-tris(p-tolyl)hexahydro-s-triazine
• 英文别名: 1,3,5-tri-p-tolyl-1,3,5-triazinane；1,3,5-tris(4-methylphenyl)-hexahydro-s-triazine；s-Triazine, hexahydro-1,3,5-tri-p-tolyl-；1,3,5-tris(4-methylphenyl)-1,3,5-triazinane
• CAS: 6639-47-0
• 化学式: C₂₄H₂₇N₃
• 分子量: 357.498
• InChiKey: UAJWDYLSRSNGFH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.8
• 重原子数：
  27
• 可旋转键数：
  3
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  9.7
• 氢给体数：
  0
• 氢受体数：
  3

安全信息

• 海关编码：
  2933699090

反应信息

• 作为反应物：
  描述：

  六氢-1,3,5-三(4-甲基苯基)-1,3,5-三嗪 生成 4-methyl-N-methyleneaniline
  参考文献：
  名称：

  Giumanini, Angelo G.; Verardo, Giancarlo; Zangrando, Ennio, Journal fur praktische Chemie (Leipzig 1954), 1987, vol. 329, # 6, p. 1087 - 1103

  摘要：

  DOI：
• 作为产物：
  描述：

  bis(4-methylphenylamino)methane 在 乙醇 作用下， 生成 六氢-1,3,5-三(4-甲基苯基)-1,3,5-三嗪
  参考文献：
  名称：

  The Political Role of the Internet in Societies in Transition: Russia and Ukraine Compared

  摘要：

  Our research investigates the opportunities provided by the Internet for political parties to communicate to the electorate, and the extent to which party websites are used versus other information sources on the Web. We find that parties in Parliament, major parties and newly created parties are more prominent online than others, and, based on standard quality indicators, that parliamentary parties and new parties have better quality websites. This confirms some of the findings concerning parties online in established democracies. On comparing party with news websites, however, we find that sites of online-only newspapers are the most popular; that online versions of offline news outlets are of secondary importance, in contrast to what has been found in established democracies; and that party and politician websites are of least importance to users, based on the number of hits to these websites. The political role of the Internet in Russia and Ukraine is discussed in conclusion.

  DOI：

  10.1177/1354068803009001720
• 作为试剂：
  描述：

  2-萘酚 在 六氢-1,3,5-三(4-甲基苯基)-1,3,5-三嗪 、 sodium ethanolate 作用下， 生成 1,1-亚甲基-2-萘酚
  参考文献：
  名称：

  SOME REACTIONS OF METHYLENE-BIS-AMINES AS AMMONO-ALDEHYDES

  摘要：

  DOI：

  10.1021/jo01195a006

文献信息

• Novel oxidative nitrogen to carbon rearrangement found in the conversion of anilines to benzaldoximes by treating with HCHO/H2O2
  作者：Naval Kapuriya、Kalpana Kapuriya、Narsinh M. Dodia、Yi-Wen Lin、Rajesh Kakadiya、Chao-Ting Wu、Ching-Huang Chen、Yogesh Naliapara、Tsann-Long Su

  DOI：10.1016/j.tetlet.2008.03.033

  日期：2008.4

  Novel rearrangement was found by reacting anilines with HCHO/H2O2 resulting in the synthesis of various benzaldoximes. The mechanism of the rearrangement is proposed and suggested that the rearrangement might proceed via unstable N-phenyloxazirane intermediate followed by the transfer of aryl moiety from nitrogen to carbon atom leading to the formation of benzaldoxime.

  通过使苯胺与HCHO / H 2 O 2反应，发现了新颖的重排反应，从而合成了各种苯甲醛肟。提出了重排的机理，并提出重排可能通过不稳定的N-苯基恶嗪烷中间体进行，然后芳基部分从氮转移到碳原子，从而导致苯甲醛肟的形成。
• Activation Relay on Rhodium-Catalyzed C–H Aminomethylation in Cooperation with Photoredox Catalysis
  作者：Ruixing Liu、Jiaxin Liu、Yin Wei、Min Shi

  DOI：10.1021/acs.orglett.9b01261

  日期：2019.6.7

  A site selective C–H aminomethylation at indole’s C3 position has been achieved by merging rhodium(III)-catalyzed C–H activation and photoredox catalysis in a one-pot manner. An investigation of the mechanistic insights rationalized the essence of the activation relay and the combination mode.

  通过以一锅方式合并铑（III）催化的C–H活化和光氧化还原催化，已实现了吲哚C3位置的位点选择性C–H氨基甲基化。对机械洞察力的研究使激活继电器和组合模式的本质合理化。
• Tetrahydro-1,3,5-thiadiazin-4-one derivative
  申请人：Nihon Nohyaku Co., Ltd.

  公开号：US04159328A1

  公开（公告）日：1979-06-26

  A tetrahydro-1,3,5-thiadiazin-4-one represented by the general formula, ##STR1## wherein R.sup.1, R.sup.2 and R.sup.3, which may be the same or different, represent each an alkyl group, allyl group, cycloalkyl group, alkoxyalkyl group, benzyl group, phenyl group or substituted phenyl group having as substituents alkyl groups, nitro group, halogen atoms, alkoxy groups, or trifluoromethyl group and R.sup.2 and R.sup.3 may also represent hydrogen atoms, is a new compound and useful for controlling insects and mites.

  由通用公式表示的1,3,5-噻二嗪-4-酮，其中R1、R2和R3相同或不同，每个代表一个烷基、烯丙基、环烷基、烷氧基烷基、苄基、苯基或取代的苯基，取代基可以是烷基、硝基、卤素原子、烷氧基或三氟甲基，R2和R3还可以代表氢原子，这是一个新化合物，用于控制昆虫和螨虫。
• A General Synthesis of Bis(<i>o</i>-azaheteroaryl)methane Derivatives from<i>N</i>-Oxides of Azines and Azoles
  作者：Magdalena Szpunar、Rafał Loska

  DOI：10.1002/ejoc.201500072

  日期：2015.4

  A general method of preparation of derivatives of bis(o-azaheteroaryl)methanes from aromatic N-oxides is reported, the key step of which is a 1,3-dipolar cycloaddition between N-oxides of azines or azoles and in situ generated terminal difluoroalkenes containing an o-azaheteroaryl substituent at the double bond. Selected products were applied for the preparation of two novel unsymmetrical analogues

  报道了一种从芳香族 N-氧化物制备双 (o-氮杂杂芳基) 甲烷衍生物的通用方法，其关键步骤是 吖嗪或唑的 N-氧化物与原位生成的末端二氟烯烃之间的 1,3-偶极环加成反应在双键上含有一个邻氮杂杂芳基取代基。选定的产品用于制备两种新型 BODIPY 荧光染料的不对称类似物，其中包含咪唑和喹啉或异喹啉单元。
• 一种手性α-季碳-α-羟基-β-氨基酮衍生物及 其合成方法
  申请人：华东师范大学

  公开号：CN109896969B

  公开（公告）日：2021-12-07

  本发明公开了一种手性α‑季碳‑α‑羟基‑β‑氨基酮的合成方法，以醇、重氮化合物及1,3,5‑三芳基‑1,3,5‑三嗪为原料，Rh2(esp)2为催化剂，手性磷酸(CPA)作为共催化剂，在有机溶剂中，分子筛为添加剂，经过一步三组分反应高立体选择性、高收率的得到产物。本发明的方法具有原子经济性高、立体选择性好、反应条件温和、收率高、操作简单安全等优点。实现了羟基叶立德的不对称胺甲基化反应，合成了一系列光学纯的α‑季碳‑α‑羟基‑β‑氨基酮衍生物。