CAS: 21714-35-2; 1-(2-Chloro-5-(Trifluoromethyl)Phenyl)Thiourea

该化合物是一种硫尿衍生物,其特点是氯和三氟甲基代苯组,这增强了其在有机合成中的活性和选择性,该化合物作为生产三环化合物,药品和农用化学物的中间体,具有特别宝贵的价值;三氟甲基组的存在有助于提高脂质和代谢稳定性,使其在药用化学应用中有用;其硫尿组织是进一步功能化的多用途建筑块,能够合成硫卓和其他含有硫磺的循环;该化合物具有良好的热稳定性,通常在标准实验室条件下处理,但鉴于其潜在毒性,应当采取适当的预防措施.

结构式图片

上下游产品

ammonium thi°Cyanate 3-amino-4-chlorobenzotrifluoride N-(2-chloro-5-(trifluoromethyl)phenylcarbamothioyl)benzamide N-(2-chloro-5-(trifluoromethyl)phenyl)cyanamide

合成工艺路线路线简述

  • 合成目标产物 (2-Chloro-5-Trifluoromethyl)Phenylthiourea 主要起始原料 3-Amino-4-Chlorobenzotrifluoride
  • (文献来源)合成步骤主要原料 3-Amino-4-Chlorobenzotrifluoride
📜3-氨基-4-氯三氟甲苯置于sodium Hydroxide体系中,用 水,丙酮 用作溶剂,化学反应 21.33H,反应生成1-(2-氯-5-三氟甲苯基)-2-硫脲
参考文献:N'-3-(Trifluoromethyl)Phenyl Derivatives Of N-Aryl-N'-Methylguanidines As Prospective Pet Radioligands For The Open Channel Of The N-Methyl-D-Aspartate (Nmda) Receptor: Synthesis And Structure-affinity Relationships
标题:N'-3-(Trifluoromethyl)Phenyl Derivatives Of N-Aryl-N'-Methylguanidines As Prospective Pet Radioligands For The Open Channel Of The N-Methyl-D-Aspartate (Nmda) Receptor: Synthesis And Structure-affinity Relationships
摘要:N-Methyl-D-Aspartate (Nmda) Receptor Dysfunction Has Been Linked To Several Neuropsychiatric Disorders,Including Alzheimer'S Disease,Epilepsy,Drug Addiction,And Schizophrenia. A Radioligand That Could Be Used With Pet To Image And Quantify Human Brain. Nmda Receptors In The Activated "Open Channel" State Would Be Useful For Research On Such Disorders And For The Development Of Novel Therapies,: To Date,No Radioligands Have Shown Well-Validated Efficacy For Imaging Nmda Receptors In Human Subjects. In Order To Discover Improved Radioligands For Pet Imaging,We Explored Structure Affinity Relationships In N'-3-(Trifluoromethyl)Phenyl Derivatives Of N-Aryl-N'-Methylguanidines,Seeking High Affinity And Moderate Lipophilicity,Plus Necessary Amenability For Labeling With A Positron-Emitter,Either Carbon-11 Or Fluorine-18. Among A Diverse Set Of 80 Prepared N'-3-(Trifluoromethyl)Phenyl Derivatives,Four Of These Compounds (13,19,20,And 36) Displayed Desirable Low Nanomolar Affinity For Inhibition Of [h-3](+)-Mk801 At The Pcp Binding Site And Are Of Interest For Candidate Pet Radioligand Development.
Doi:10.1021/acs.Jmedchem.5B01510

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✅ COA系统入驻 | 共享模式

主要参考文献

参考标题:Parallel Solution-Phase Synthesis Of A 2-Aminothiazole Library Including Fully Automated Work-Up
作者:Hans-Peter Buchstaller,Uwe Anlauf |发布日期:2011.2.1
摘要:And Effective Procedure For The Solution Phase Preparation Of A 2-Aminothiazole Combinatorial Library Is Described. Reaction, Work-Up And Isolation Of The Title Compounds As Free Bases Was Accomplished In A Fully Automated Fashion Using The Chemspeed Asw 2000 Automated Synthesizer. The Compounds Were Obtained In Good Yields And Excellent Purities Without Any Further Purification Procedure.

合成参考文献

参考DOI号:10.1021/acs.jmedchem.5b01510
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