CAS: 119-34-6; 4-Amino-2-Nitrophenol

相似化合物

137-09-7 603-87-2 577-72-0

上下游产品

2,4-Dinitrophenol 3-nitrophenyl azide N-(4-hydroxy-3-nitrophenyl)acetamide 2-nitro-4-azidophenol 4-diazo-2-nitrophenol N-(4-hydroxy-3-nitrophenyl)acetamide N-acetyl-sulfanilic acid-(4-hydroxy-3-nitro-anilide)N-acetyl-sulfanilic acid-(4-hydroxy-3-nitro-anilide) (4-Hydroxy-3-nitrophenyl)trimethylammonium Iodide

📜2,4-二硝基酚置于sodium Tetrahydroborate体系中,用 水 用作溶剂,化学反应 0.03H,反应生成2-硝基-4-氨基苯酚
参考文献:Magnetically Recoverable Gold Nanorods As A Novel Catalyst For The Facile Reduction Of Nitroarenes Under Aqueous Conditions
标题:Magnetically Recoverable Gold Nanorods As A Novel Catalyst For The Facile Reduction Of Nitroarenes Under Aqueous Conditions
摘要:In This Work,Cysteine-Functionalized Fe3O4@carbon Magnetic Nanoparticles Were Used For The Synthesis Of Gold Nanorods. Fe3O4@c Nanoparticles Were First Prepared By Synthesis Of Fe3O4 Magnetic Nanoparticles (Mnps),And Then Carbon-Coated Mnps (Fe3O4@c) Were Synthesized By Glucose Carbonization Using A Hydrothermal Method. Finally,The Gold Nrs Were Loaded On The Modified Surface Of Fe3O4@c Mnps. The Designed Magnetically Recoverable Gold Nanorods,After Full Characterization By Ftir,Sem,Tem,Tga,Vsm,Xrd,And Icp-Oes,Were Applied To The Reduction Of Nitroarenes. The Fe3O4@c@cys-Au Nanorods Showed Higher Performance Than Fe3O4@c@cys-Au Nanospheres In A Selective Facile Reduction Of Nitroarenes To The Corresponding Aminoarenes In Aqueous Medium At Room Temperature Using Nabh4.[graphics].
Doi:10.1007/s10562-016-1921-4

专利信息

专利号:US-7550510-B2
优先权日:2001-07-06
标 题 :Solid phase synthesis of arylretinamides
发明人：CURLEY JR ROBERT W; MERSHON SERENA M; BARNETT DEREK W; CLAGETT-DAME MARGARET; CHAPMAN JASON S
权利人:WISCONSIN ALUMNI RES FOUND
摘要:A solid phase synthetic method for preparing arylretinamides is provided. The method comprises reacting hexachloroacetone with a solvent-suspended resin-bound triphenylphosphine to provide a suspension comprising an activated chlorinating reagent; reacting retinoic acid with the activated chlorinating reagent to provide retinoyl chloride; adding pyridine and a select arylamine to the resulting mixture; and stirring the resulting mixture for a time and at a temperature sufficient for the select arylamine to react with the retinoyl chloride and provide the arylretinamide. Also provided, are select arylretinamides that can be prepared by the present method, and methods of using such arylretinamides to induce apoptosis in cancer cells.

专利号:US-2004102650-A1
优先权日:2001-07-06
标 题:Solid phase synthesis of arylretinamides

专利号:US-2003105164-A1
优先权日:2001-07-06
标 题 :Solid phase synthesis of arylretinamides

专利号:WO-03003987-A2
优先权日:2001-07-06
标题:Solid phase synthesis of arylretinamides

专利号:US-6696606-B2
优先权日:2001-07-06
标 题 :Solid phase synthesis of arylretinamides

专利号:US-2009137566-A1
优先权日:2005-05-26
标 题 :Substituted Piperdines as Renin Inhibitors
发明人：EHARA TAKERU; HITOMI YUKO; KONISHI KAZUHIDE; MASUYA KELICHI
权利人:EHARA TAKERU; HITOMI YUKO; KONISHI KAZUHIDE; MASUYA KELICHI
摘要:The invention relates to substituted 3,4- or higher substituted piperididine compounds, the use thereof for the preparation of a pharmaceutical formulation for the treatment of a disease that depends on activity of renin; the use of a compound of that class in the treatment of a disease that depends on activity of renin; these compounds for use in the diagnostic and therapeutic treatment of a warm-blooded animal, especially for the treatment of a disease (=disorder) that depends on activity of renin; pharmaceutical formulations or products comprising said compounds, and/or a method of treatment comprising administering said compounds, a method for the manufacture of said compounds, as well as novel intermediates, starting materials and/or partial steps for their synthesis. The compounds preferably have the formula I, n n n n n n n n n n wherein the moieties R1, R2, R11 and W are as defined in the specification.