CAS: 1269291-95-3; 1-(3-Fluorophenyl)-1H-Pyrazole-4-Carbonitrile

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      3-fluorophenylhydrazine hydr°Chloride 5-amino-1-(3-fluorophenyl)-1H-pyrazole-4-carbonitrile m-fluorophenylhydrazine 1-(3-fluorophenyl)-1H-pyrazole 4-(4,5-dihydro-1H-imidazol-2-yl)-1-(3-fluorophenyl)-1H-pyrazole

      合成工艺路线路线简述

        📜(3-氟苯基)肼置于盐酸,盐酸羟胺,三氟乙酸,Sodium Iodide体系中,用 乙醇,N,N-二甲基甲酰胺 用作溶剂,化学反应 19.0H,反应生成1-(3-氟苯基)-1H-吡唑-4-腈
        参考文献:Synthesis,Docking Studies,Pharmacological Activity And Toxicity Of A Novel Pyrazole Derivative (Lqfm 021)-possible Effects On Phosphodiesterase
        标题:Synthesis,Docking Studies,Pharmacological Activity And Toxicity Of A Novel Pyrazole Derivative (Lqfm 021)-possible Effects On Phosphodiesterase
        摘要:本研究描述了lqfm 021的合成路线和分子计算对接,并考察了其生物学效果和毒性.对接研究显示,Lqfm 021与磷酸二酯酶-3(pde-3)之间存在强相互作用.在分离动脉中,内皮的存在增强了lqfm 021的舒张作用,而抑制环核苷酸则减少了舒张作用.用kcl(45 Mm)预收缩后,处理四乙基铵(tea)(5 Mm)和抑制网状ca2+-Atp酶也显示对舒张有抑制作用.此外,该化合物降低了因ca2+内流引起的收缩.急性毒性测试表明,该化合物几乎无毒.综上所述,本研究表明一种新的吡唑合成衍生物可能是pde-3抑制剂,具有血管舒张活性和低毒性.
        Doi:10.1248/cpb.C12-01016

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        ✅ COA系统入驻 | 共享模式

        主要参考文献

        参考标题:A Convenient Synthesis Of Pyrazole‐imidazoline Derivatives By Microwave Irradiation
        作者:Getúlio Rosa,Bernardo A. Souto,Cynthia N. Pereira,Bruna C. Teixeira,Maurício S. Santos |发布日期:2019.6
        摘要:Synthesized By A New Methodology Using Microwave Irradiation, In Short Time (20-30 Min), In Low Power (50-70 W), And In 34-92% Yield. Among All Methodologies Evaluated, No Side Products Were Obtained. All Derivatives Were Completely Characterized By Ft-Ir, 1H And 13C Nmr, Gc-Ms, And Hrms.

        合成参考文献

        参考DOI号:10.1248/cpb.c12-01016
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