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5-(4-methoxyphenyl)-1,2,4-triazolidine-3-thione

中文名称
——
中文别名
——
英文名称
5-(4-methoxyphenyl)-1,2,4-triazolidine-3-thione
英文别名
5-(4-Methoxyphenyl)-1,2,4-triazolidine-3-thione
5-(4-methoxyphenyl)-1,2,4-triazolidine-3-thione化学式
CAS
——
化学式
C9H11N3OS
mdl
——
分子量
209.272
InChiKey
KXYNPCDXQVDIKT-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

计算性质

  • 辛醇/水分配系数(LogP):
    1.1
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    77.4
  • 氢给体数:
    3
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    4-甲氧基苯甲醛氨基磺酸一水合肼 作用下, 以 乙醇 为溶剂, 反应 0.58h, 生成 5-(4-methoxyphenyl)-1,2,4-triazolidine-3-thione
    参考文献:
    名称:
    A novel one pot multi-component strategy for facile synthesis of 5-aryl-[1,2,4]triazolidine-3-thiones
    摘要:
    We have disclosed an efficient, one pot, novel multi-component approach for the synthesis of 5-aryl-[1,2,4]triazolidine-3-thiones from aldehyde, hydrazine hydrate, and trimethylsilyl isothiocyanate (TMSNCS) in the presence of catalytic amount of sulfamic acid. High yields, easy work-up procedure, no chromatographic separation, and novelty in multi-component strategy are the main merits of the present strategy. (C) 2014 Published by Elsevier Ltd.
    DOI:
    10.1016/j.tetlet.2014.10.052
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文献信息

  • Envirocat EPZ-10: An Efficient Catalyst for the Synthesis of 1,2,4- Triazolidine-3-thiones
    作者:Pradeep M. Mhaldar、Dattaprasad M. Pore
    DOI:10.2174/1570178616666191019144317
    日期:2020.3.25
    <p>A simple and environmentally benign room temperature synthesis of 1,2,4-triazolidine-3- thiones is described using Envirocat EPZ-10R as a solid acid catalyst in the aqueous medium. The use of Envirocat EPZ-10R as a green catalyst, reusability of the catalyst, water as a universal solvent and good yields of the product are the attractive features of the present method.</p> </sec></div> <div class="value-text ch">描述了在室温下使用Envirocat EPZ-10R作为固体酸催化剂在水介质中合成1,2,4-三唑啉-3-硫酮的简单且环保的方法。使用Envirocat EPZ-10R作为绿色催化剂、催化剂的可重复使用性、水作为通用溶剂以及产品产率高是该方法的吸引人特点。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">[C16MPy]AlCl3Br: an efficient novel ionic liquid for synthesis of novel 1,2,4-triazolidine-3-thiones in water</div> <div class="value"> <div class="value-text"> <span>作者:</span>Jayavant D. Patil、Dattaprasad M. Pore </div> <div class="value-text"> <span>DOI:</span>10.1039/c3ra46916f </div> <div class="value-text"> <span>日期:</span>—— </div> <div class="value-text en">4-triazolidine-3-thiones in water at ambient temperature. A variety of aldehydes undergo smooth reaction with <span style='color:#ff0000'>thiosemicarbazide</span> and <span style='color:#ff0000'>substituted</span> <span style='color:#ff0000'>thiosemicarbazides</span>. In the case of <span style='color:#ff0000'>substituted</span> <span style='color:#ff0000'>thiosemicarbazides</span> the <span style='color:#ff0000'>corresponding</span> 1,2,4-triazolidine-3-thiones are obtained as products instead of <span style='color:#ff0000'>1,3,4-oxadiazoles</span>. A broad variety of functional groups are tolerated and a large number of substrates can be applied</div> <div class="value-text ch">一种高效的新型离子液体,[C 16 MPy] AlCl 3溴已被合成并作为催化剂在环境温度下于水中生态合成新型的1,2,4-三唑烷-3-硫酮。各种醛与硫代氨基脲和取代的硫代氨基脲进行平滑反应。在取代的硫代氨基脲的情况下,获得相应的1,2,4-三唑烷-3-硫酮而不是1,3,4-恶二唑的产物。可以容忍各种各样的官能团,并且可以使用该协议应用大量底物。快速,环保的反应具有高收率,使用环境温度和水作为溶剂,简便的后处理步骤以及产物分离,出色的催化剂可回收性,高原子经济性,离子液体的新颖性和方案该协议的辅助优势。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">Synthesis of triazolidines and triazole using DMAP</div> <div class="value"> <div class="value-text"> <span>作者:</span>Devidas A. Mali、Vikas N. Telvekar </div> <div class="value-text"> <span>DOI:</span>10.1080/00397911.2016.1263338 </div> <div class="value-text"> <span>日期:</span>2017.2.16 </div> <div class="value-text en">ABSTRACT An efficient methodology has been developed for the <span style='color:#ff0000'>synthesis</span> of 1,2,4-triazolidine-3-thione and 3-ethoxy-5-phenyl-4H-1,2,4 triazole <span style='color:#ff0000'>using</span> N,N-dimethylpyridine-4-amine (DMAP). Aldehydes and thiosemicarbazide were reacted in water at ambient temperature in presence of DMAP and provided corresponding products in good to moderate yield. GRAPHICAL ABSTRACT</div> <div class="value-text ch">摘要 开发了一种使用 N,N-二甲基吡啶-4-胺合成 1,2,4-三唑烷-3-硫酮和 3-乙氧基-5-苯基-4H-1,2,4 三唑的有效方法( DMAP)。醛和氨基硫脲在环境温度下在 DMAP 存在下在水中反应,并以良好至中等产率提供相应的产物。图形概要</div> </div> </li> <li class="feature-list-item"> <div class="content-title">Sm2O3/Fluoroapatite as a reusable catalyst for the facile, green, one-pot synthesis of triazolidine-3-thione derivatives under aqueous conditions</div> <div class="value"> <div class="value-text"> <span>作者:</span>Surya Narayana Maddila、Suresh Maddila、Kranthi Kumar Gangu、Werner E. van Zyl、Sreekantha B. Jonnalagadda </div> <div class="value-text"> <span>DOI:</span>10.1016/j.jfluchem.2017.01.012 </div> <div class="value-text"> <span>日期:</span>2017.3 </div> <div class="value-text en">A <span style='color:#ff0000'>new</span> series of fourteen triazolidine-3-thione derivatives (11 compounds) were synthesized <span style='color:#ff0000'>via</span> the <span style='color:#ff0000'>reaction</span> of aromatic aldehydes with thiosemicarbazide with samaria loaded fluorapatite, (Sm2O3/FAp) as catalyst in aqueous media. Fluoroapatite proved superior as support relative to hydroxyapatite in terms of improved yield and reduced <span style='color:#ff0000'>reaction</span> time. The <span style='color:#ff0000'>new</span> catalyst, Sm/FAp was characterized by various</div> <div class="value-text ch">在含水介质中,以芳香族醛类与硫代氨基脲与负载am草的氟磷灰石(Sm 2 O 3 / FAp)为催化剂,合成了一系列新的十四个三唑烷-3-硫酮衍生物(11种化合物)。相对于羟基磷灰石,氟磷灰石被证明在提高产率和减少反应时间方面作为载体更好。新的催化剂Sm / FAp通过多种仪器技术进行了表征,包括XRD,SEM,TEM和BET。催化剂易于分离和重复使用七次,而活性没有明显降低。报告的策略具有许多优点,例如易于制备,绿色溶剂,缩短了反应时间,出色的产品收率(92%至97%)以及操作简便。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">Effect of precursor pH on structural, magnetic and catalytic properties of CoFe2O4@SiO2 green nanocatalyst</div> <div class="value"> <div class="value-text"> <span>作者:</span>Pranav P. Bardapurkar、Sunil S. Shewale、Sandeep A. Arote、Shreyas S. Pansambal、Nilesh P. Barde </div> <div class="value-text"> <span>DOI:</span>10.1007/s11164-020-04366-7 </div> <div class="value-text"> <span>日期:</span>2021.5 </div> <div class="value-text en">structure at pH 9. <span style='color:#ff0000'>Magnetic</span> parameters show <span style='color:#ff0000'>effects</span> due to γ-Fe2O3 phase and pH. Effect on catalytic <span style='color:#ff0000'>properties</span> was investigated for the synthesis of 5-(4-chlorophenyl)-1,2,4-triazolidine-3-thione. <span style='color:#ff0000'>Structural</span> and morphological changes due to change in pH were found to enhance the catalytic yield considerably. Exquisiteness of the material as a catalyst is that it is <span style='color:#ff0000'>magnetically</span> separable and can be</div> <div class="value-text ch">摘要 铁氧体钴是用于许多治疗应用,光催化,气体检测器,高密度数据存储等的有前途的材料。工艺参数的优化在调整其性能方面起着至关重要的作用。目前的工作报道了前驱体pH对分散在二氧化硅中的钴铁氧体纳米粒子性能的影响。随着pH值的增加,微晶尺寸显示从16nm增加到18.5nm。在较低的前体pH下观察到许多不良相。晶格参数和粒度分布显示出对pH的显着影响。二氧化硅基质表现在其结构中,在pH 9的磁参数表明由于作用给高孔隙率结构重大变化了γ-Fe 2 ö 3相和pH。研究了5-(4-氯苯基)-1,2,4-三唑烷-3-硫酮对催化性能的影响。发现由于pH的变化引起的结构和形态变化大大提高了催化产率。该材料作为催化剂的精妙之处在于它是磁性可分离的并且可以连续重复使用,从而使其成为一种经济,绿色的催化剂。 图形概要</div> </div> </li> </ul> <a href="https://chem.molaid.com/material/detail?source=UserSourcePortal&id=30fd5e5yfbbb842e56M0&inchikey=KXYNPCDXQVDIKT-UHFFFAOYSA-N" target="_blank" rel="nofollow" class="view-more">查看更多</a> </div> <div class="module" id="tongleihuahewu"> <h3 class="module-title"><i class="iconfont icon-tongleihuahewu"></i>同类化合物</h3> <div class="compounds-list"> <a target="_blank" href="https://www.molaid.com/MS_152" class="compound-item" 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class="module-title"><i class="iconfont icon-xiangguanjiegoufenlei"></i>相关结构分类</h3> <div class="compounds-list"> <a href="https://www.molaid.com/fenzi/10" class="compound-item" title="有机杂环化合物">有机杂环化合物</a> <a href="https://www.molaid.com/fenzi/11" class="compound-item" title="苯类化合物">苯类化合物</a> <a href="https://www.molaid.com/fenzi/12" class="compound-item" title="木脂素、新木脂素和相关化合物">木脂素、新木脂素和相关化合物</a> <a href="https://www.molaid.com/fenzi/13" class="compound-item" title="苯丙烷和聚酮">苯丙烷和聚酮</a> <a href="https://www.molaid.com/fenzi/14" class="compound-item" title="脂质和类脂质分子">脂质和类脂质分子</a> <a href="https://www.molaid.com/fenzi/15" class="compound-item" title="有机酸及其衍生物">有机酸及其衍生物</a> <a href="https://www.molaid.com/fenzi/16" class="compound-item" title="有机氧化合物">有机氧化合物</a> <a href="https://www.molaid.com/fenzi/17" class="compound-item" title="生物碱及其衍生物">生物碱及其衍生物</a> <a href="https://www.molaid.com/fenzi/18" class="compound-item" title="有机硫化合物">有机硫化合物</a> <a href="https://www.molaid.com/fenzi/19" class="compound-item" title="核苷、核苷酸和类似物">核苷、核苷酸和类似物</a> <a href="https://www.molaid.com/fenzi/20" class="compound-item" title="碳氢化合物衍生物">碳氢化合物衍生物</a> <a href="https://www.molaid.com/fenzi/21" class="compound-item" title="有机氮化合物">有机氮化合物</a> <a href="https://www.molaid.com/fenzi/22" class="compound-item" title="碳氢化合物">碳氢化合物</a> <a href="https://www.molaid.com/fenzi/23" class="compound-item" title="有机卤素化合物">有机卤素化合物</a> <a href="https://www.molaid.com/fenzi/24" class="compound-item" title="有机聚合物">有机聚合物</a> <a href="https://www.molaid.com/fenzi/25" class="compound-item" title="有机金属化合物">有机金属化合物</a> <a href="https://www.molaid.com/fenzi/26" class="compound-item" title="乙炔化物 ">乙炔化物 </a> <a href="https://www.molaid.com/fenzi/27" class="compound-item" title="有机磷化合物">有机磷化合物</a> <a href="https://www.molaid.com/fenzi/28" class="compound-item" title="叠烯">叠烯</a> <a href="https://www.molaid.com/fenzi/29" class="compound-item" title="有机1,3-偶极化合物">有机1,3-偶极化合物</a> <a href="https://www.molaid.com/fenzi/30" class="compound-item" title="碳化物">碳化物</a> <a href="https://www.molaid.com/fenzi/31" class="compound-item" title="有机盐">有机盐</a> <a href="https://www.molaid.com/fenzi/32" class="compound-item" title="有机阳离子">有机阳离子</a> <a href="https://www.molaid.com/fenzi/33" class="compound-item" title="卡宾">卡宾</a> <a href="https://www.molaid.com/fenzi/34" class="compound-item" title="有机阴离子">有机阴离子</a> </div> </div> </div> <div class="right"> <div class="module"> <link rel="stylesheet" href="https://www.molaid.com/assets/css/common/hot-molecular.css?v=202504271"> <div class="component-card hot-molecular-card" style="--color: #FF4539;"> <div class="title"> <h3 class="title-name">热门分子</h3> </div> <div class="card-content"> <ul class="list"> <li class="item item-special" data-sort="TOP"> <div class="item-img"> <img src="data:image/svg+xml;base64,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