首页> 中文期刊>结构化学 >Synthesis, X-ray Structure and Bioactivity of N-4-Methyl-1,2,3-thiadiazole-5-carbonyl-N'-3,5- dichloro-4-(1,1,2,2-tetrafluoroethoxyl)phenyl Urea

Synthesis, X-ray Structure and Bioactivity of N-4-Methyl-1,2,3-thiadiazole-5-carbonyl-N'-3,5- dichloro-4-(1,1,2,2-tetrafluoroethoxyl)phenyl Urea

     

摘要

The title compound N-4-methyl-1,2,3-thiadiazole-5-carbonyl-N'-3,5-dichloro-4- (1,1,2,2- tetrafluoroethoxyl)phenyl urea (C13H8Cl2F4N4O3S, Mr = 447.19) has been synthesized from 4-methyl- 1,2,3-thiadiazole-5-carbonyl chloride as the starting material, and its structure was characterized by proton Nuclear Magnetic Resonance (1H NMR), Infra Red Spectroscopy (IR), high-resolution mass spectroscopy (HRMS), and single-crystal X-ray diffraction. The crystal of the title compound belongs to triclinic, space group Pi with a = 6.0780(8), b = 11.3760(14), c = 12.1440(18) A, α = 96.887(7), β = 91.027(12), γ= 104.252(13)°, Z = 2, V= 806.98(19)A3, Dc = 1.840 g/cm3, μ= 0.601 mm-1, F(000) = 448, R = 0.0450 and wR = 0.0869. X-ray analysis indicates that the 1,2,3-thiadiazole ring is not coplanar with the phenyl ring, and the dihedral angle is 33.57°. Two intermolecular hydrogen bonds N(2)-H…O(1 ), S(1 )…H-C(11), and three weak intermolecular interactions, C(11)…O(1), N(1)…O(2) and S…O(1), are observed. The bioassay results indicate that the title compound has good insecticidal activity against Culex pipiens pallens and good induction activity for tobacco against tobacco mosaic virus which is equal to that of TDL.

著录项

  • 来源
    《结构化学》|2012年第12期|1721-1728|共8页
  • 作者单位

    State Key Laboratory of Elemento Organic Chemistry, Nankai University, Tianjin 300071, China;

    The Ural Federal University Named after the First President ofRussia B. N. Yeltsin, Yeltsin UrFU 620002, Ekaterinburg, Russia;

    State Key Laboratory of Elemento Organic Chemistry, Nankai University, Tianjin 300071, China;

    State Key Laboratory of Elemento Organic Chemistry, Nankai University, Tianjin 300071, China;

    State Key Laboratory of Elemento Organic Chemistry, Nankai University, Tianjin 300071, China;

    State Key Laboratory of Elemento Organic Chemistry, Nankai University, Tianjin 300071, China;

    Sichuan Functional Heterocyclic Compounds Engineering Technology Research Center, Lier Chemicals Co., Ltd., No. 97 Mianxingdonglu, Mianyang, Sichuan 621000, China;

    The Ural Federal University Named after the First President ofRussia B. N. Yeltsin, Yeltsin UrFU 620002, Ekaterinburg, Russia;

    The Ural Federal University Named after the First President ofRussia B. N. Yeltsin, Yeltsin UrFU 620002, Ekaterinburg, Russia;

    The Ural Federal University Named after the First President ofRussia B. N. Yeltsin, Yeltsin UrFU 620002, Ekaterinburg, Russia;

  • 原文格式 PDF
  • 正文语种 chi
  • 中图分类 间硫氮茂(噻唑);
  • 关键词

    生物活性; 噻二唑; 苯基脲; 羰基; 合成; 结构; 抗烟草花叶病毒; 单晶X-射线衍射;

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