CAS: 13505-01-6; 3-Fluoro-4-Nitropyridine

该化合物是有机化合物,其特征是氟原子和附于环的硝基化合物,分子结构由六人组成的芳香环组成,内含5个碳原子和1个氮原子,其中氟替代体位于3点,硝基组位于4点.该化合物一般是黄色至褐色固体,其极性因电阴性氟素和硝基组而闻名,可影响其再活性和溶性,经常用于有机合成,并用作生产药品和农用化学品的一种中间体.该硝基组的存在还可能带来某些生物活动,使其对医药化学感兴趣.在处理该化合物时,应采取安全防范措施,因为该化合物可能构成健康风险,包括毒性和环境危害.

结构式图片

相似化合物

2247-88-3 769-54-0 1805578-52-2

欧盟法规

ECHA物质C&L通报

上下游产品

3-bromo-4-nitropyridine (S)-tert-butyl (1-(4-nitropyridin-3-yl)piperidin-3-yl)carbamate N-(3-(1H-pyrazol-1-yl)pyridin-4-yl)-2,3-dichlorobenzenesulfonamide 3-fluoro-pyridin-4-ylamine

合成工艺路线路线简述

  • 合成目标产物 3-Fluoro-4-Nitropyridine 主要起始原料 3-Bromo-4-Nitropyridine
  • (文献来源)合成步骤主要原料 3-Bromo-4-Nitropyridine
📜3-溴-4-硝基吡啶置于四丁基氟化铵体系中,用 四氢呋喃,二甲基亚砜 用作溶剂,化学反应生成3-氟-4-硝基吡啶,3-溴-4-氟吡啶
参考文献:Synthesis Of Meta-Substituted [18F]-3-Fluoro-4-Aminopyridines By Direct Radiofluorination Of Pyridine N-Oxides
标题:Synthesis Of Meta-Substituted [18F]-3-Fluoro-4-Aminopyridines By Direct Radiofluorination Of Pyridine N-Oxides
摘要:本文披露了一种用于含有至少一个脱离基团的芳香n-杂环n-氧化物的氟化方法.这些n-氧化物可以被还原为氟化芳香n-杂环胺类似物.这种新颖的氟化方法可以成功地用于合成标记有18F的芳香n-杂环化合物.

海关参考信息

专利信息


专利号:US-2017355648-A1
优先权日:2016-04-26
标题 :Synthesis of meta-substituted [18f]-3-fluoro-4-aminopyridines by direct radiofluorination of pyridine n-oxides

专利号:US-10160695-B2
优先权日:2016-04-26
标 题 :Synthesis of meta-substituted [18F]-3-fluoro-4-aminopyridines by direct radiofluorination of pyridine N-oxides
发明人:BRUGAROLAS PEDRO
权利人:UNIV CHICAGO
摘要:Disclosed herein are methods for the fluorination aromatic N-heterocyclic N-oxides that comprise at least one leaving group. The N-oxides may be reduced to the fluorinated aromatic N-heterocyclic amine analogs. This novel fluorination approach may be successfully applied for synthesizing aromatic N-heterocyclic compounds labeled with 18 F.

专利号:US-8362019-B2
优先权日:2008-02-01
标 题:Synthesis and anti-proliferative effect of substituted imidazo[4,5-b]pyrazine compounds
发明人:WINFIELD LEYTE L
权利人:SPELMAN COLLEGE; WINFIELD LEYTE L
摘要:This invention provides for compounds, compositions, and methods that involve anti-proliferative and anti-neoplastic activity in cancer cells. In particular, a series of benzimidazole, purine, imidazopyridine, and imidazopyrizine compounds having selected substitution patterns are disclosed, and the activity of various subject compounds is demonstrated. In particular, the disclosure provides for substituted imidazo[4,5-b]pyrazine compounds having the general formula n ntheir salts, pharmaceutical compositions, and methods of treatment using the subject compounds and compositions.

专利号:US-2012095009-A1
优先权日:2008-02-01
标题 :Synthesis and anti-proliferative effect of benzimidazole derivatives

专利号:US-2012095037-A1
优先权日:2008-02-01
标题:Synthesis and anti-proliferative effect of benzimidazole derivatives

专利号:US-8334302-B2
优先权日:2008-02-01
标题:Synthesis and anti-proliferative effect of substituted imidazo[4,5-b]pyridine compounds

供应商参考报价(招募中)

品牌试剂参考报价(招募中)

📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式
📝 需求与反馈
尽可能描述清楚需求与问题信息
×

通知