N-(p-methoxyphenyl)dithiocarbamic acid | 15867-08-0

• 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: N-(p-methoxyphenyl)dithiocarbamic acid
• 英文别名: (4-methoxy-phenyl)-dithiocarbamic acid；(4-Methoxy-phenyl)-dithiocarbamidsaeure；(4-Methoxyphenyl)carbamodithioic acid
• CAS: 15867-08-0
• 化学式: C₈H₉NOS₂
• mdl: MFCD24390354
• 分子量: 199.298
• InChiKey: XKXOWGIMYHPMBF-UHFFFAOYSA-N

物化性质

• 沸点：
  293.8±42.0 °C(Predicted)
• 密度：
  1.311±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  12
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.125
• 拓扑面积：
  54.4
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  N-(p-methoxyphenyl)dithiocarbamic acid 在 盐酸 、 aluminum oxide 、 sodium monochloroacetic acid 作用下， 以 水 为溶剂， 反应 4.03h， 生成 methyl (R)-4-((5R,8S,9S,10R,13R,14S,17R)-3,6-bis(2-((4-methoxyphenyl)carbamothioyl)hydrazineylidene)-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoate
  参考文献：
  名称：

  Synthesis of new hyodeoxycholic acid thiosemicarbazone derivatives under solvent-free conditions using microwave

  摘要：

  An efficient and simple method for synthesis of new hyodeoxycholic acid thiosemicarbazone derivatives under solvent-free conditions using microwave has been developed. Its main advantages are short reaction times, good conversions and the environmentally friendly nature of the process. The preliminary results indicate that some of these compounds possess inhibitory effects against E. coli. (C) 2010 Zhi Gang Zhao. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.

  DOI：

  10.1016/j.cclet.2010.10.020
• 作为产物：
  描述：

  二硫化碳 、 甲氧苯胺 以 乙腈 为溶剂， 反应 0.17h， 生成 N-(p-methoxyphenyl)dithiocarbamic acid
  参考文献：
  名称：

  通过铜催化的分子内C-H活化反应从异氰酸酯，苯胺和杂异丙苯一锅合成高功能化的苯并[1,3]噻嗪

  摘要：

  室温下，通过异氰酸酯，苯胺和异枯烯在铜中的铜催化多组分反应，开发了一种一锅法合成的官能化苯并噻嗪衍生物。使用温和的铜催化反应条件下，过渡金属催化的C-H键活化，使用简单易用的起始原料，无需柱色谱即可获得高收率的纯净产品，这是所用方法的主要优点，其中包括使用的其他方法。以此目的。通过光谱（1 H和13 C-NMR，IR和EI-MS）并通过元素分析确认了结构。

  DOI：

  10.1002/jccs.201800493

文献信息

• Solvent-Free Synthesis of Indole-Based Thiosemicarbazones under Microwave Irradiation
  作者：Lingling Liu、Jie Yang、Zhigang Zhao、Peiyu Shi、Xingli Liu

  DOI：10.3184/030823410x12628833270368

  日期：2010.1

  A rapid, efficient and environmentally friendly methodology has been developed for the synthesis of indole-3-carboxaldehyde thiosemicarbazones by using aluminum oxide as the solid support under microwave assisted solvent-free conditions. Compared with the conventional heating method, this method gave the target products in good yield.

  开发了一种快速、高效且环保的方法，用于在微波辅助无溶剂条件下以氧化铝为固体载体合成吲哚-3-甲醛缩氨基硫脲。与常规加热方法相比，该方法得到的目标产物收率良好。
• Design, Synthesis and Antiproliferative Activities of Diaryl Thiourea Derivatives as Anticancer Agents
  作者：Jianwen Yao、Zuopeng He、Jing Chen、Daquan Chen、Wei Sun、Wenfang Xu

  DOI：10.1002/cjoc.201200708

  日期：2012.10

  Two new series of diaryl thiourea containing sorafenib derivatives 9a–9t were designed and synthesized, and their antiproliferative activities against PC‐3, HCT116 and MDA‐MB‐231 cell lines were evaluated. All compounds generally showed antiproliferative activity to PC‐3 cells, most of the analogs exhibited potent antiproliferative activity to HCT116 cells, and compounds 9e, 9f, 9o and 9p demonstrated

  设计并合成了两个新的含索拉非尼衍生物9a - 9t的二芳基硫脲系列产品，并评估了它们对PC-3，HCT116和MDA-MB-231细胞系的抗增殖活性。所有化合物通常对PC-3细胞均具有抗增殖活性，大多数类似物均对HCT116细胞具有有效的抗增殖活性，化合物9e，9f，9o和9p对所有这三种细胞系均具有抑制活性。所有新合成的化合物的结构均通过1 H NMR，13 C NMR和HRMS确定。
• Design, synthesis and biological evaluation of thiourea and nicotinamide-containing sorafenib analogs as antitumor agents
  作者：Xiangkai Kong、Zeyu Yao、Zuopeng He、Wenfang Xu、Jianwen Yao

  DOI：10.1039/c4md00536h

  日期：——

  Thiourea and nicotinamide-containing sorafenib analogs with better antiproliferative and anti-angiogenic activities than sorafenib were well designed and synthesized.

  硫脲和烟酰胺含量比索拉非尼更好的抗增殖和抗血管生成活性的类索拉非尼类似物已经被设计和合成。
• Efficient Preparation of Isothiocyanates From Dithiocarbamates Using Bromineless Brominating Reagent
  作者：Ramesh Yella、Harisadhan Ghosh、Siva Murru、Santosh K. Sahoo、Bhisma K. Patel

  DOI：10.1080/00397910903219476

  日期：2010.6.25

  determined. Utilizing this thiophilic bromineless brominating agent EDPBT, highly useful synthetic intermediates (alkyl and aryl isothiocyanates) have been achieved directly from dithiocarbamates. EDPBT can be easily prepared from readily available reagents. It has been used as a thiophilic reagent, and its thiophilicity dominates over its brominating ability for substrates amenable to bromination. This

  首次确定了双溴化物试剂 1,1'-(乙烷-1,2-二基)二吡啶鎓双溴化物 (EDPBT) 的晶体结构。利用这种亲硫性无溴溴化剂 EDPBT，可以直接从二硫代氨基甲酸酯获得非常有用的合成中间体（异硫氰酸烷基酯和芳基酯）。EDP​​BT 可以很容易地用现成的试剂制备。它已被用作亲硫试剂，对于适合溴化的底物，其亲硫性优于其溴化能力。这是制备异硫氰酸酯的可持续过程，因为用过的试剂可以回收、再生和重复使用。
• Microwave-Assisted Synthesis of New Steroidal Thiosemicarbazones Derived from methyl 3-Oxocholanate under Solvent-Free Conditions
  作者：Zhigang Zhao、Xingli Liu、Lingling Liu、Guohua Li

  DOI：10.3184/030823410x12798092457988

  日期：2010.8

  A series of novel steroidal thiosemicarbazones derived from methyl 3-oxocholanate were synthesised in good yields via microwave irradiation under solvent-free conditions. The structures of the compounds were confirmed by spectroscopic data. Compared to the conventional method, microwave irradiation was a fast and simple method. These compounds were tested for antibacterial activity against S. aureus, S. pyogenes, and E. coli bacteria.

  在无溶剂条件下，通过微波辐照合成了一系列新型甾体硫代氨基甲酸甲酯。光谱数据证实了这些化合物的结构。与传统方法相比，微波辐照是一种快速而简单的方法。测试了这些化合物对金黄色葡萄球菌、化脓性葡萄球菌和大肠杆菌的抗菌活性。