CAS: 82105-88-2; (4-Ethoxybenzyl)Triphenylphosphonium Bromide
该化合物是一种四硝基铵盐,其特点是有正电磷离子和一种对溴的反作用,其结构特征是三联苯组和一个苯基甲基苯基组的中磷原子结合,其特性是其独特的特性.该化合物通常用于有机合成,并作为一种分阶段转移催化剂,因为它能够促进分期转移离子.它显示出有机溶剂的溶性,这增强了其在各种化学反应中的效用.乙氧组的存在可影响其再活性和溶性,使其适合有机化学的应用.此外,溴离子是一种反作用,可以相互反应,允许合成途径的多用途.应当参考安全数据,因为四硝基铵化合物能够表现出毒性和环境持久性.
- 英文名称(4-Ethoxybenzyl)Triphenylphosphonium Bromide
- 中文名称(4-乙氧基苄基)三苯基溴化鏻
- IUPAC名称(4-ethoxybenzyl)triphenylphosphonium bromide
- 其它别名(4-乙氧基苄基)三苯基溴化膦; Phosphonium, [(4-Ethoxyphenyl)Methyl]Triphenyl-, Hydrobromide
- CAS编号82105-88-2
- MFCD编号:MFCD00011834
- EINECS号:617-299-4
- 分子式:C27H26BrOP分子量:477.38
- 产品CID: 1812748
- 产品分类有机原料→分子砌块→芳环类化合物→苯类化合物
物理性质
MSDS等安全信息
欧盟法规
ECHA物质C&L通报REACH预注册上下游产品
4-ethoxybenzyl bromide triphenylphosphine合成工艺路线路线简述
- 10031-82-0 = 82105-88-2
反应条件:1.1 Reagents: Sodium Borohydride Solvents: Methanol; 30 Min,0 °C2.1 Reagents: N-Bromosuccinimide,Triphenylphosphine Solvents: Dichloromethane; 0 °C; 15 Min,60 °C; 60 °C -> Rt2.2 30 Min,60 °C3.1 Solvents: Tetrahydrofuran; 0 °C; 2 H,85 °C
标题:Methoxy-Naphthyl-Linked N-Benzyl Pyridinium Styryls As Dual Cholinesterase Inhibitors: Design,Synthesis,Biological Evaluation,And Structure-Activity Relationship
作者:Abdullaha,Mohd; Et Al
参考文献:Acs Omega 日期:2023 卷标:8(20) 页码:17591-17608]
2606-57-7 = 82105-88-2
反应条件:1.1 Solvents: Tetrahydrofuran; 0 °C; 2 H,85 °C
标题:Methoxy-Naphthyl-Linked N-Benzyl Pyridinium Styryls As Dual Cholinesterase Inhibitors: Design,Synthesis,Biological Evaluation,And Structure-Activity Relationship
作者:Abdullaha,Mohd; Et Al
参考文献:Acs Omega 日期:2023 卷标:8(20) 页码:17591-17608]
6214-44-4 = 82105-88-2
反应条件:1.1 Reagents: N-Bromosuccinimide,Triphenylphosphine Solvents: Dichloromethane; 0 °C; 15 Min,60 °C; 60 °C -> Rt1.2 30 Min,60 °C2.1 Solvents: Tetrahydrofuran; 0 °C; 2 H,85 °C
标题:Methoxy-Naphthyl-Linked N-Benzyl Pyridinium Styryls As Dual Cholinesterase Inhibitors: Design,Synthesis,Biological Evaluation,And Structure-Activity Relationship
作者:Abdullaha,Mohd; Et Al
参考文献:Acs Omega 日期:2023 卷标:8(20) 页码:17591-17608
📜4-甲基苯乙醚置于n-溴代丁二酰亚胺(Nbs)体系中,用 Xylene 作为反应溶剂,化学反应生成 4-乙氧苄基三苯基溴化膦
参考文献:Alkoxylated P-Phenylenevinylene Oligomers: Synthesis And Spectroscopic And Electrochemical Properties
标题:Alkoxylated P-Phenylenevinylene Oligomers: Synthesis And Spectroscopic And Electrochemical Properties
摘要:Twenty-One N-Alkoxy Substituted Phenylenevinylene Oligomers Were Synthesized,Varying In Size,Number And Position Of The Or Groups. Ir,Ms And Solubility Data Are Presented. NMR Measurements Provided The Molecular Structure As Well As Information About Conformations And Molecular Dynamics. Uv And Of Cyclic Voltammetric Data Give Correlations Of Chemical Structure (Number And Position Of Or Substituents) With Separate Homo And Lumo Energies. (C) 1997 Elsevier Science Ltd.
DOI:10.1016/s0040-4020(97)00871-5
海关参考信息
- 2902300000-甲苯
2908199090-其他酚的卤化衍生物
2908999090-其他酚的硝化衍生物
2918290000-其他含酚基羧酸 - 💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
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合成参考文献
参考DOI号:10.1016/S0040-4020(97)00871-5
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