CAS: 17252-51-6; 4,4-Trimethylenedipyridine

该化合物其结构特征为结构结构,由三甲基乙烯(-CH2-CH2-CH2-2)桥连接的两只环虫,通常在室温时是一种固体,由于有有助于其稳定性和再活性的环而以其芳香特性而闻名;它溶于各种有机溶剂,使其在有机合成和化学协调中有用; 环中氮原子的存在使分子具有基本性,使其能够参与各种化学反应,包括与金属离子的协调.此外,4,4'-三甲基二甲酰丙烯可展示有趣的电子特性,使其成为材料科学和催化应用的候选物.在处理和储存时,应参考安全数据,如任何化学物质,以确保采取适当的预防措施.

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CAS号100-43-6 4-乙烯基吡啶 | CAS号108-89-4 4-甲基吡啶 | CAS号16898-52-5 1,3-二(4-哌啶基)丙烷 | CAS号34049-15-5 1,3-双(4-吡啶 1-氧化物)丙烷 | CAS号16898-52-5 1,3-二(4-哌啶基)丙烷 | CAS号61736-46-7 1-methyl-4-[3-(...

合成工艺路线路线简述

  • 合成目标产物 4,4'-Trimethylenedipyridine 主要起始原料 4-Vinylpyridine And 4-Methylpyridine
  • (文献来源)合成步骤主要原料 4-Vinylpyridine 和 4-Methylpyridine
📜1,3-二(4-哌啶基)丙烷置于silica Gel,钯体系中,化学反应 3.0H,反应生成4,4'-(1,3-丙二基)双吡啶
参考文献:The Effect Of Substitution On The Utility Of Piperidines And octahydroindoles For Reversible Hydrogen Storage
标题:The Effect Of Substitution On The Utility Of Piperidines And octahydroindoles For Reversible Hydrogen Storage
摘要:替代哌啶和八氢吲哚在可逆有机储氢液方面,作为氢燃料电池的实用性进行了比较.理论高斯计算表明哪些结构特征可能会降低脱氢焓.实验结果显示,将电子供体或共轭取代基连接到哌啶环上大大提高了催化脱氢速率,其中4-氨基哌啶和哌啶-4-甲酰胺的速率最高.观测到了一些不希望的副反应,例如在4-二甲氨基哌啶脱氢过程中发生的烷基转移反应,4-烷氧基和4-氨基吲哚氢化和/或随后脱氢过程中发生的c-O和c-N断裂反应,以及4-氨基吡啶氢化过程中发生的歧化反应.
Doi:10.1039/b718209K

海关参考信息

专利信息


专利号:US-8735586-B2
优先权日:2007-06-26
标 题 :Regioselective copper catalyzed synthesis of benzimidazoles and azabenzimidazoles
发明人:ALONSO JORGE; LINDENSCHMIDT ANDREAS; NAZARÉ MARC; URMANN MATTHIAS; HALLAND NIS; RKYEK OMAR
权利人:ALONSO JORGE; LINDENSCHMIDT ANDREAS; NAZARÉ MARC; URMANN MATTHIAS; HALLAND NIS; RKYEK OMAR; SANOFI SA
摘要:The present invention relates to a process for the regioselective synthesis of compounds of the formula I, n nwherein R0; R1; R2; R3; R4; R5; A1; A2; A3; A4, Q and J have the meanings indicated in the claims. The present invention provides a direct copper catalyzed regioselective process to a wide variety of unsymmetrical, multifunctional N-substituted benzimidazoles or azabenzimidazoles of formula I starting from 2-halo-nitroarenes and N-substituted amides.

专利号:EP-2173747-B1
优先权日:2007-06-26
标 题:A regioselective metal catalyzed synthesis of annelated benzimidazoles and azabenzimidazoles
发明人:ALONSO JORGE; LINDENSCHMIDT ANDREAS; NAZARE MARC; R KYEN OMAR; URMANN MATHIAS; HALLAND NIS
权利人:SANOFI SA
摘要:The present invention relates to a process for the regioselective synthesis of compounds of the formula I, wherein R1; R2; R3; R4; J1; J2; J3; J4 and G have the meanings indicated in the claims. The present invention provides a direct metal, e.g. palladium or copper, catalyzed, regioselective process to a wide variety of unsymmetrical, multifunctional N-substituted benzimidazoles or azabenzimidazoles of formula I starting from 2-halo-nitroarenes and N-substituted amides.

专利号:US-9303056-B2
优先权日:2012-07-25
标题 :Monomer for synthesis of RNA, method for producing same, and method for producing RNA
发明人:KATAOKA MASANORI
权利人:UNIV KOCHI
摘要:The objective of the present invention is to provide a monomer for RNA synthesis which can be efficiently produced and therefore by which the producing cost of RNA can be remarkably decreased, and a method for efficiently producing the monomer in a small number of steps. In addition, the objective of the present invention is also to provide a method by which RNA can be efficiently produced even when a approximately stoichiometry amount of the monomer for RNA synthesis is used. The monomer for RNA synthesis according to the present invention is represented by the following formula (I) or (I′): n nwherein R 1 is a protective group of the hydroxy group and R 2 is an alkyl group or the like.

专利号:US-2022089618-A1
优先权日:2019-01-29
标题:Solid-State Synthesis Of Precursors Of Metal-Organic Frameworks
发明人:MAJANO GERARDO J; FALKOWSKI JOSEPH M
权利人:EXXONMOBIL RES & ENG CO
摘要:Metal-organic frameworks (MOFs) are highly porous entities comprising a multidentate ligand coordinated to multiple metal atoms, typically as a coordination polymer. MOFs are usually produced from a solvent in powder form under hydrothermal or solvothermal synthesis conditions. Alternately, powder-form precursors of MOFs may be formed by milling or mulling a substantially solid mixture of a metal salt and a multidentate organic ligand, optionally in the presence of a small amount of a solvent. The powder-form precursors may then undergo heating, typically in the absence of applied shear, to produce the corresponding MOF. Mulling may be differentiated from milling at least in that mulling applies to the substantially solid mixture at a non-constant pressure and milling applies a constant pressure while forming the powder-form precursor. In some cases, mulling may promote more effective formation of the powder-form precursor compared to milling.

专利号:US-12054833-B2
优先权日:2020-07-29
标 题:Catalyst for synthesizing organic carbonate and method of producing thereof, electrode for synthesizing organic carbonate, cell for synthesizing organic carbonate, method of producing organic carbonate, and synthesis system
发明人:FUJINUMA NAOHIRO
权利人:SEKISUI CHEMICAL CO LTD
摘要:An organic carbonate synthesis catalyst for electrochemically synthesizing an organic carbonate from carbon monoxide, comprises: an active particle containing a metal element; and a porous carbon supporting the active particle.

专利号:US-2010261909-A1
优先权日:2007-06-26
标题 :Regioselective copper catalyzed synthesis of benzimidazoles and azabenzimidazoles

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合成参考文献


参考文献:10.1107/s1600536811015819
摘要:Liu GX, Xu XY. trans-Tetra-aqua-bis-[1,3-bis-(4-pyrid-yl)propane-κN]cobalt(II) biphenyl-4,4'-disulfonate monohydrate. Acta Crystallogr Sect E Struct Rep Online. 2011 May 01;67(Pt 5):m651–2.
参考文献:10.1107/s1600536811018563
摘要:Kuyinu O, Purdy AP, Butcher RJ. Sulfonated 1,3-bis-(4-pyrid-yl)propane. Acta Crystallogr Sect E Struct Rep Online. 2011 Jun 01;67(Pt 6):o1534.
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