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4-(三氟甲基)烟酰胺的高效液相色谱分析
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作者 张凯 郭勇飞 +2 位作者 潘理想 李乐乐 张小军 《世界农药》 CAS 2023年第11期22-25,共4页
建立一种可对4-(三氟甲基)烟酰胺进行含量测定的高效液相色谱方法。采用Agilent C18色谱柱为固定相和二极管阵列检测器,在波长266nm条件下,以甲醇-0.5%冰乙酸水溶液(体积比20∶80)为流动相,对4-(三氟甲基)烟酰胺样品的含量进行定量分析... 建立一种可对4-(三氟甲基)烟酰胺进行含量测定的高效液相色谱方法。采用Agilent C18色谱柱为固定相和二极管阵列检测器,在波长266nm条件下,以甲醇-0.5%冰乙酸水溶液(体积比20∶80)为流动相,对4-(三氟甲基)烟酰胺样品的含量进行定量分析。该方法中的线性相关系数(R^(2))为0.9999,标准偏差为0.25,变异系数为0.25%,平均回收率为100.25%。该方法线性关系良好,具有准确度高、重现性好、分离效果好等优点,适用于4-(三氟甲基)烟酰胺的定量分析和质量控制。 展开更多
关键词 4-(三氟甲基)烟酰胺 高效液相色谱 分析
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Synthesis and Crystal Structure of N-[(3aR,4R,4aR,5aS,6S,6aS)-1,3-Dioxooctahydro-4,6-ethenocyclopropa[f]isoindol-2(1H)-yl]-3-(trifluoromethyl)phenylmethanimine
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作者 周辛波 谢云德 +2 位作者 钟武 王建柏 李松 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2010年第8期1231-1235,共5页
The crystal structure of the title compound(C19H15F3N2O2,Mr = 360.33) was determined by single-crystal X-ray diffraction.The crystal belongs to triclinic,space group P1,with a = 6.5604(7),b = 13.9614(16),c = 18.... The crystal structure of the title compound(C19H15F3N2O2,Mr = 360.33) was determined by single-crystal X-ray diffraction.The crystal belongs to triclinic,space group P1,with a = 6.5604(7),b = 13.9614(16),c = 18.1790(18) ,α = 102.749(7),β = 97.542(6),γ = 94.355(4)°,V = 1600.5(3) 3,Z = 4,Dc = 1.495 g/cm3,λ(MoKα) = 0.71070,F(000) = 744,μ(MoKα) = 0.122 mm-1,R = 0.0434 and wR = 0.1051.A total of 7590 unique reflections were collected,of which 5429 with |F|2 ≥ 2σ|F|2 were observed.The two cyclohexene rings in the molecule adopt boat-boat conformations with the deviations of ring atoms C(9) and C10 from the C(5)/C(6)/C(7)/C(8) plane(Ⅰ) by 1.1204(0.0023) and 1.1132(0.0023) ,respectively,whereas from the C(2)/C(3)/C(5)/C(8) plane(Ⅱ) by 1.1627(0.0022) and 1.1818(0.0021) ,respectively.In the cyclopropane and lactam rings,atoms C(11) and N(1) point towards the double bond of C(9)-C(10) and the dihedral angle between the ring plane(Ⅲ) containing C(1),C(2),C(3) and C(4) and plane(IV) consisting of C(6),C(7) and C(11) is 55.76(0.07)°.The dihedral angles between planes Ⅳ and Ⅰ and Ⅱ and Ⅲare 63.58(0.07)° and 58.10(0.06)°,respectively.The dihedral angle between the benzene ring C(13)~ C(18) and plane Ⅳ is 42.41(0.06)°. 展开更多
关键词 N-[(3aR 4R 4aR 5aS 6S 6aS)-1 3-dioxooctahydro-4 6-ethenocyclopropa[f]isoin-dol-2(1H)-yl]-3-trifluoromethyl)phenylmethanimine crystal structure synthesis
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Design, synthesis and insecticidal activities of novel 1-substituted-5-(trifluoromethyl)-1H-pyrazole-4-carboxamide derivatives 被引量:1
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作者 Zhi-Bing Wu Xiang Zhou +2 位作者 Yi-Qiang Ye Pei-Yi Wang Song Yang 《Chinese Chemical Letters》 SCIE CAS CSCD 2017年第1期121-125,共5页
A series of novel 5-(trifluoromethyl)-1H-pyrazole-4-carboxamide derivatives(6a–6n, 7a, 7b, and 8a-8f)were synthesised by placing the amide bond at the 4-position of the pyrazole ring. These derivatives differed f... A series of novel 5-(trifluoromethyl)-1H-pyrazole-4-carboxamide derivatives(6a–6n, 7a, 7b, and 8a-8f)were synthesised by placing the amide bond at the 4-position of the pyrazole ring. These derivatives differed from the structure of chlorantraniliprole analogues with the amide bond at the 5-position of the pyrazole ring. Preliminary bioassay results revealed that a few title compounds exhibited good insecticidal activities against lepidopteran pests, such as Plutella xylostella, Mythimna separate, Heliothis armigera, and Ostrinia nubilalis. Some title compounds also elicited broad-spectrum insecticidal activities against dipterous insects including Culex pipiens pallens after altering the amide position. Similar to pyrazole-5-carboxamide analogues, compounds 6b and 6e showed 100% insecticidal activity against P. xylostella, C. pipiens pallens, and M. separate at concentrations of 200, 2, and 200 mg/m L, respectively.This finding suggested that 5-(trifluoromethyl)-1H-pyrazole-4-carboxamide derivatives are potential alternative insecticides for management of agriculture pests. 展开更多
关键词 5-trifluoromethyl - 1H-pyrazole-4-carboxamide Insecticidal activities Chlorantraniliprole Ryanodine receptors
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Synthesis and Herbicidal Activity of Novel N-(2-Fluoro-5(3- methyl-2,6-dioxo-4-(trifluoromethyl)-2,3-dihydro-pyrimidin- l(6H)-yl)phenyl)-2-phenoxyacetamide Derivatives 被引量:1
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作者 吴道新 孙炯 +7 位作者 黄明智 莫洪波 王晓光 李宏伟 任叶果 胡志彬 何莲 尹笃林 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2011年第11期2401-2406,共6页
Thirteen novel N-(2-fluoro-5-(3-methyl-2,6-dioxo-4-(trifluoromethy)-2,3-dihydropyrimidin-1(6H)-yl)phenyl)- 2-phenoxy)acetamides were designed and synthesized utilizing 4-fluoro-aniline and ethyl 3-amino-4,4,4... Thirteen novel N-(2-fluoro-5-(3-methyl-2,6-dioxo-4-(trifluoromethy)-2,3-dihydropyrimidin-1(6H)-yl)phenyl)- 2-phenoxy)acetamides were designed and synthesized utilizing 4-fluoro-aniline and ethyl 3-amino-4,4,4-trifluoro-but-2-enoate as starting materials. The chemical structures of all compounds were confirmed by IH NMR, IR, mass spectrum and elemental analyses. Subsequently, the herbicidal activities of the as-prepared compounds were evalu-ated in the greenhouse. Bioassay results indicated that most of compounds had better herbicidal activities against dicotyledonous weeds. Among all the tested compounds, compounds 4a--4i showed good herbicidal activities at both pre-emergence and post-emergence treatment against two or three kinds of dicotyledonous weeds, such as Abutilon theophrasti Medic, Amaranthus ascendens L, and Chenopodium album L at the dosage of 75 g ai/ha. 展开更多
关键词 synthesis design 2 6-dioxo-4-trifluoromethyl-2 3-dihydropyrimidine N-phenyl-2-phenoxyacetamide SYNTHESIS herbicidal activity
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吡唑化合物pyr3干预对压力负荷诱导的大鼠左心室肥厚的影响 被引量:3
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作者 田小芍 陈明 刘春霞 《中国循环杂志》 CSCD 北大核心 2013年第3期226-229,共4页
目的:探讨瞬时受体电位通道C亚族3亚型(TRPC3)的选择性阻滞剂吡唑化合物Ethyl-1-(4-f2,3,3一trichloroacrylamide)phenyl)-5-(trifluoromethyl)-1H—pyrazole-4-carboxylate(pyr3)的体内干预对压力负荷大鼠左心室肥厚(LvH... 目的:探讨瞬时受体电位通道C亚族3亚型(TRPC3)的选择性阻滞剂吡唑化合物Ethyl-1-(4-f2,3,3一trichloroacrylamide)phenyl)-5-(trifluoromethyl)-1H—pyrazole-4-carboxylate(pyr3)的体内干预对压力负荷大鼠左心室肥厚(LvH)程度的影响。方法:采用腹主动脉缩窄手术建立左心压力负荷模型。30只200—240g雄性SD大鼠随机分为五组(n=6):假手术对照组、手术对照组、假手术后全程给药组、手术后后期给药组,手术后全程给药组。6周后,计算各组大鼠左心室质量指数、左心室心肌细胞横径,逆转录多聚酶连反应(RT—PCR)、免疫组织化学和蛋白免疫印迹检测TRPC3和钙调神经磷酸酶A13信使核糖核酸(mRNA)和蛋白的表达水平。结果:与假手术对照组相比,手术对照组左心室肥厚相关指标(左心室质量指数和左心室心肌细胞横径)及TRPC3、钙调神经磷酸酶AB蛋白和mRNA的表达显著升高;假手术后全程给药组左心室肥厚相关指标无显著变化,而TRPC3和钙调神经磷酸酶AB蛋白及mRNA的表达量显著升高,差异均有统计学意义(P均〈0.05)。与手术对照组比较,手术后全程给药组左心室肥厚相关指标、TRPC3及钙调神经磷酸酶A13蛋白和mRNA表达均明显降低(P均〈0.05);手术后后期给药组左心室肥厚相关指标及钙调神经磷酸酶AB蛋白和mRNA的表达下降,差异均有统计学意义(P均〈0.05),而TRPC3的蛋白和mRNA表达未见显著降低。结论:pyr3体内干预能够一定程度上阻止压力负荷导致的大鼠左心室肥厚,降低压力负荷大鼠左心室TRPC3和钙调神经磷酸酶AB表达的上调。 展开更多
关键词 Ethyl-1-(4-(2 3 3-trichloroacrylamide)phenyl)-5-(trifluoromethyl)-1H—pyrazole-4-carboxylate 压力负荷 左心室肥厚 瞬时受体电位通道C亚族3亚型 钙调神经磷酸酶Aβ
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