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5-(3-chlorophenyl)-4-(4-fluorophenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione | 720667-75-4

中文名称
——
中文别名
——
英文名称
5-(3-chlorophenyl)-4-(4-fluorophenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione
英文别名
5-(3-Chlorophenyl)-4-(4-fluorophenyl)-4H-1,2,4-triazole-3-thiol;3-(3-chlorophenyl)-4-(4-fluorophenyl)-1H-1,2,4-triazole-5-thione
5-(3-chlorophenyl)-4-(4-fluorophenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione化学式
CAS
720667-75-4
化学式
C14H9ClFN3S
mdl
——
分子量
305.763
InChiKey
LUYNRRWMVKSISV-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):
    3.9
  • 重原子数:
    20
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    59.7
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    聚合甲醛5-(3-chlorophenyl)-4-(4-fluorophenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione乙醇 为溶剂, 反应 0.5h, 以76%的产率得到5-(3-chlorophenyl)-4-(4-fluorophenyl)-2-hydroxymethyl-2,4-dihydro-3H-1,2,4-triazole-3-thione
    参考文献:
    名称:
    Halogen Substituents as an Effective Modulators of Antibacterial Activity of Substituted 1,2,4-triazole-3-thiones
    摘要:
    Fourteen novel compounds were obtained and their chemical structures were established by H-1-NMR and IR spectra as well as elemental analyses. As one of the most important factors determining the changes of activity of respective fluorophenyl and iodophenyl derivatives, one should consider the volume of halogen substituent and its influence on the lipophilicity of the entire molecule.
    DOI:
    10.2174/157018012804586987
  • 作为产物:
    描述:
    1-(3-chlorobenzoyl)-4-(4-fluorophenyl)thiosemicarbazide 在 sodium hydroxide 作用下, 反应 2.0h, 以90%的产率得到5-(3-chlorophenyl)-4-(4-fluorophenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione
    参考文献:
    名称:
    Studies on the Anticonvulsant Activity and Influence on GABA-ergic Neurotransmission of 1,2,4-Triazole-3-thione- Based Compounds
    摘要:
    本研究测试了几种 1,2,4-三唑-3-硫酮衍生物对小鼠最大电休克诱发癫痫发作的抗惊厥活性。所有活性化合物的特点都是起效迅速、作用持久。结构-活性观察结果表明,当 1,2,4-三唑核上连接的苯基环中至少有一个在对位上具有取代基时,化合物具有抗惊厥活性的几率要高得多。此外,研究结果还让我们得出结论:尽管洛雷克唑(第二代抗惊厥药物)和标题化合物的结构相似,但它们的抗惊厥活性是通过完全不同的分子机制实现的。
    DOI:
    10.3390/molecules190811279
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文献信息

  • Synthesis and antimicrobial activity of thiosemicarbazides, s-triazoles and their Mannich bases bearing 3-chlorophenyl moiety
    作者:Tomasz Plech、Monika Wujec、Agata Siwek、Urszula Kosikowska、Anna Malm
    DOI:10.1016/j.ejmech.2010.11.010
    日期:2011.1
    efficient synthesis of some 1,4-disubstituted thiosemicarbazide derivatives is described. The reaction of 3-chlorobenzoic acid hydrazide with various aryl isothiocyanates gave thiosemicarbazide derivatives (1–11) in good yield. The cyclization of compounds (1–11) in the presence of 2% NaOH resulted in the formation of compounds (12–22) containing the 1,2,4-triazole ring. A series of new Mannich bases (23–33)
    描述了一些1,4-二取代的硫代氨基脲衍生物的快速有效的合成。的3-氯苯甲酸酰肼与各种芳基异硫氰酸酯反应,得到氨基硫脲衍生物(1 - 11以良好的收率)。化合物(的环化1 - 11)在2%的NaOH的存在导致在化合物(形成12 - 22),其含有1,2,4-三唑环。还合成了与1,2,4-三唑结构有关的一系列新的曼尼希碱(23 – 33)。所有这些化合物均经过体外测试对有氧细菌参考菌株的抗菌活性-6革兰氏阳性和3革兰氏阴性; 还检查了12株金黄色葡萄球菌临床分离株。试图阐明取代基的性质/位置对所述化合物的抗菌活性的影响。
  • Surface Modified Metal Nano-Particle and Use Thereof
    申请人:LEE Sang Joon
    公开号:US20120168681A1
    公开(公告)日:2012-07-05
    The present invention provides a metal nanoparticle that is surface-modified with a hydrophilic or hydrophobic functional group, and a composition for optical detection comprising the same. The surface-modified nanoparticles according to the present invention form clusters suitable for optical detection, for example, suitable as an X-ray contrast agent, and have surface plasmon energy in the visible region, thereby being usefully applied to a variety of optical detection methods.
  • US8753895B2
    申请人:——
    公开号:US8753895B2
    公开(公告)日:2014-06-17
  • Halogen Substituents as an Effective Modulators of Antibacterial Activity of Substituted 1,2,4-triazole-3-thiones
    作者:Tomasz Plech、Monika Wujec、Urszula Kosikowska、Anna Malm
    DOI:10.2174/157018012804586987
    日期:2012.12.1
    Fourteen novel compounds were obtained and their chemical structures were established by H-1-NMR and IR spectra as well as elemental analyses. As one of the most important factors determining the changes of activity of respective fluorophenyl and iodophenyl derivatives, one should consider the volume of halogen substituent and its influence on the lipophilicity of the entire molecule.
  • Studies on the Anticonvulsant Activity and Influence on GABA-ergic Neurotransmission of 1,2,4-Triazole-3-thione- Based Compounds
    作者:Tomasz Plech、Barbara Kaproń、Jarogniew Łuszczki、Monika Wujec、Agata Paneth、Agata Siwek、Marcin Kołaczkowski、Maria Żołnierek、Gabriel Nowak
    DOI:10.3390/molecules190811279
    日期:——
    The anticonvulsant activity of several 1,2,4-triazole-3-thione derivatives on mouse maximal electroshock-induced seizures was tested in this study. Characteristic features of all active compounds were rapid onset of action and long lasting effect. Structure-activity observations showed that the probability of obtaining compounds exerting anticonvulsant activity was much higher when at least one of the phenyl rings attached to 1,2,4-triazole nucleus had a substituent at the para position. The obtained results, moreover, permit us to conclude that despite the structural similarity of loreclezole (second-generation anticonvulsant drug) and the titled compounds, their anticonvulsant activity is achieved via completely different molecular mechanisms.
    本研究测试了几种 1,2,4-三唑-3-硫酮衍生物对小鼠最大电休克诱发癫痫发作的抗惊厥活性。所有活性化合物的特点都是起效迅速、作用持久。结构-活性观察结果表明,当 1,2,4-三唑核上连接的苯基环中至少有一个在对位上具有取代基时,化合物具有抗惊厥活性的几率要高得多。此外,研究结果还让我们得出结论:尽管洛雷克唑(第二代抗惊厥药物)和标题化合物的结构相似,但它们的抗惊厥活性是通过完全不同的分子机制实现的。
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