CAS: 859161-48-1; 3-(Bromomethyl)-6-Chloropyridazine
相似化合物
1121-79-5 120276-59-7 1011487-94-7MSDS等安全信息
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CAS号1121-79-5 3-氯-6-甲基哒嗪合成工艺路线路线简述
- 合成目标产物 3-Bromomethyl-6-Chloro-Pyridazine 主要起始原料 3-Chloro-6-Methylpyridazine
- 539-88-8 = 859161-48-1
反应条件:1.1 Reagents: Hydrazine Hydrate (1:1) Solvents: Ethanol2.1 Reagents: Acetic Acid,Bromine Solvents: Acetic Acid; 40 °C; 0.5 H,40 °C -> 80 °C3.1 Reagents: Sodium Acetate Solvents: Acetic Acid; 1 H,Reflux4.1 Reagents: Phosphorus Oxychloride; 3 H,60 - 65 °C; 65 °C -> Rt4.2 Reagents: Sodium Hydroxide Solvents: Water; Ph 7 - 8,Cooled5.1 Reagents: N-Bromosuccinimide Catalysts: Azobisisobutyronitrile Solvents: Carbon Tetrachloride; 10 H,Reflux
标题:Synthesis And Herbicidal Activity Of 3-(Substituted Phenoxymethyl)-6-Chloropyridazines
作者:Hu,Fang-Zhong; Et Al
参考文献:Youji Huaxue 日期:2007 卷标:27(5) 页码:593-596]
1121-79-5 = 859161-48-1
反应条件:1.1 Reagents: N-Bromosuccinimide Catalysts: Azobisisobutyronitrile Solvents: Carbon Tetrachloride; 10 H,Reflux
标题:Synthesis And Herbicidal Activity Of 3-(Substituted Phenoxymethyl)-6-Chloropyridazines
作者:Hu,Fang-Zhong; Et Al
参考文献:Youji Huaxue 日期:2007 卷标:27(5) 页码:593-596]
13327-27-0 = 859161-48-1
反应条件:1.1 Reagents: Phosphorus Oxychloride; 3 H,60 - 65 °C; 65 °C -> Rt1.2 Reagents: Sodium Hydroxide Solvents: Water; Ph 7 - 8,Cooled2.1 Reagents: N-Bromosuccinimide Catalysts: Azobisisobutyronitrile Solvents: Carbon Tetrachloride; 10 H,Reflux
标题:Synthesis And Herbicidal Activity Of 3-(Substituted Phenoxymethyl)-6-Chloropyridazines
作者:Hu,Fang-Zhong; Et Al
参考文献:Youji Huaxue 日期:2007 卷标:27(5) 页码:593-596]
94248-99-4 = 859161-48-1
反应条件:1.1 Reagents: Sodium Acetate Solvents: Acetic Acid; 1 H,Reflux2.1 Reagents: Phosphorus Oxychloride; 3 H,60 - 65 °C; 65 °C -> Rt2.2 Reagents: Sodium Hydroxide Solvents: Water; Ph 7 - 8,Cooled3.1 Reagents: N-Bromosuccinimide Catalysts: Azobisisobutyronitrile Solvents: Carbon Tetrachloride; 10 H,Reflux
标题:Synthesis And Herbicidal Activity Of 3-(Substituted Phenoxymethyl)-6-Chloropyridazines
作者:Hu,Fang-Zhong; Et Al
参考文献:Youji Huaxue 日期:2007 卷标:27(5) 页码:593-596]
5157-08-4 = 859161-48-1
反应条件:1.1 Reagents: Acetic Acid,Bromine Solvents: Acetic Acid; 40 °C; 0.5 H,40 °C -> 80 °C2.1 Reagents: Sodium Acetate Solvents: Acetic Acid; 1 H,Reflux3.1 Reagents: Phosphorus Oxychloride; 3 H,60 - 65 °C; 65 °C -> Rt3.2 Reagents: Sodium Hydroxide Solvents: Water; Ph 7 - 8,Cooled4.1 Reagents: N-Bromosuccinimide Catalysts: Azobisisobutyronitrile Solvents: Carbon Tetrachloride; 10 H,Reflux
标题:Synthesis And Herbicidal Activity Of 3-(Substituted Phenoxymethyl)-6-Chloropyridazines
作者:Hu,Fang-Zhong; Et Al
参考文献:Youji Huaxue 日期:2007 卷标:27(5) 页码:593-596
📜3-氯-6-甲基哒嗪置于n-溴代丁二酰亚胺(Nbs)体系中,用 四氯化碳 作为反应溶剂,化学反应 4.0H,反应生成 3-(溴甲基)-6-氯吡嗪
参考文献: Cmet Inhibitors[fr] Inhibiteurs De Cmet
标题: Cmet Inhibitors[fr] Inhibiteurs De Cmet
摘要:提供以下公式的化合物供与cmet一起使用:其中变量如本文所定义.还提供包含这些化合物的药物组合物,试剂盒和制造物品;用于制备这些化合物的有用中间体和方法;以及使用这些化合物的方法.
海关参考信息
- 2903399020-溴甲烷
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