CAS: 3466-32-8; 1-Bromo-4-(Methylsulfonyl)Benzene

该化合物是一种有机化合物,其特征是存在一个联苯环上附着的溴原子,以及一个甲基溴功能组;该化合物一般是白色的,是白色的,是白色的,是已知的,是其磺酰体功能组,它具有极分性质,极地溶剂中可能溶解. 溴代金可影响其反应,使其在各种化学反应中有用,包括核生殖替代. 4-溴苯甲基磺可能展示生物活动,使其对制药研究感兴趣,其特性,如熔点,沸点和溶性,可以因纯度和环境条件而不同.在处理时,应参考安全数据,因为如果摄入或吸入,可能会对健康造成危害.总的来说,该化合物是有机合成和药用化学中有价值的中间体.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

CAS号104-95-0 4-溴硫代苯甲醚 | CAS号589-87-7 对溴碘苯 | CAS号74-88-4 碘甲烷 | CAS号60822-47-1 4-Bromothioanisole | CAS号934-71-4 1-溴-4-(甲亚磺酰基)苯 | CAS号3406-73-3 2-(4-bromopheny... | CAS号108-86-1 溴苯 | CAS号7143-01-3 甲基磺酸酐 | CAS号106-53-6 4-溴苯硫酚 | CAS号105135-96-4 3-(4-methylsulf... | CAS号5470-49-5 4-甲磺酰基苯胺 | CAS号340771-31-5 1-乙炔-4-(甲基磺酰基)-苯 | CAS号21134-15-6 1-甲烷磺酰基-4-苯氧基苯 | CAS号877-66-7 4-甲磺酰基苯肼盐酸盐 | CAS号701-34-8 4-溴苯磺酰胺 | CAS号15979-81-4 4-methylsulfony... | CAS号100-25-4 对二硝基苯 | CAS号106-39-8 对氯溴苯

合成工艺路线路线简述

  • 合成目标产物 4-Bromophenyl Methyl Sulfone 主要起始原料 4-Bromothioanisole
  • (文献来源)合成步骤主要原料 4-Bromothioanisole
4-溴茴香硫醚置于双氧水体系中,用 甲醇 作为反应溶剂,化学反应生成 4-溴苯甲砜
参考文献:将金属配合物单元和氧化还原位点集成到钍基金属有机框架中,用于硫化物的选择性光催化氧化
标题:将金属配合物单元和氧化还原位点集成到钍基金属有机框架中,用于硫化物的选择性光催化氧化
摘要:使用各种金属配合物单元和钍(th)簇构建了一系列高对称性的th 6-金属有机框架(mof),然后作为明确的催化剂模型应用于甲基苯硫醚的光催化氧化反应.通过引入金属配合物单元和氧化还原位点(th 6 簇和单金属位点)来整合th 6-Mofs可以有效调节转化率和选择性.其中,Ni-Pba-Th 6 (pba = 4-吡啶-4-基苯甲酸)对甲基苯砜的转化率高达约99%,选择性约97%.实验和理论计算进一步阐明th 6 簇是甲基苯基硫醚氧化为甲基苯基砜的催化位点,而ni-Pba是过氧化氢还原的催化位点.这项工作为更高效的钍基 Mof 催化剂的结构设计和光催化应用提供了新的见解.
DOI:10.1002/adfm.202308534

海关参考信息

专利信息


专利号:US-2022135413-A1
优先权日:2020-10-30
标题:Synthesis of Ammonia Using Cycle-Generated Hydrogen Sulfide
发明人:HAMERS ROBERT; BACHMAN BENJAMIN
权利人:WISCONSIN ALUMNI RES FOUND
摘要:Improved methods of synthesizing ammonia from hydrogen sulfide and lithium nitrate are disclosed. Specifically, in a continuous cycle, hydrogen sulfide reactant is regenerated from the elemental sulfur that is extracted from a product of the ammonia synthesis, and the regenerated hydrogen sulfide is fed back into the ammonia synthesis reaction. The cycle that regenerates the hydrogen sulfide uses either a water-containing or a water and carbon-containing feedstock to facilitate the regeneration of the hydrogen sulfide from the elemental sulfur.

专利号:US-2005119332-A1
优先权日:1998-03-12
标 题 :Substituted thiophene compounds as modulators of protein tyrosine phosphatases (PTPases)
发明人:JEPPESEN LONE; ANDERSEN HENRIK S; OLSEN OLE H; JUDGE LUKE M; HOLSWORTH DANIEL D; BAKIR FARID; AXE FRANK U; GE YU
摘要:The present invention provides novel compounds of formula 1a, n nnovel compositions, methods of their use, and methods of their manufacture, where such compounds are pharmacologically useful inhibitors of Protein Tyrosine Phosphatases (PTPase's) such as PTP1B, CD45, SHP-1, SHP-2, PTPα, LAR and HePTP or the like. The compounds are useful in the treatment of type I diabetes, type II diabetes, impaired glucose tolerance, insulin resistance, obesity, immune dysfunctions including autoimmunity diseases with dysfunctions of the coagulation system, allergic diseases including asthma, osteoporosis, proliferative disorders including cancer and psoriasis, diseases with decreased or increased synthesis or effects of growth hormone, diseases with decreased or increased synthesis of hormones or cytokines that regulate the release of/or response to growth hormone, diseases of the brain including Alzheimer's disease and schizophrenia, and infectious diseases.

专利号:US-8664402-B2
优先权日:2011-03-09
标题:Process for preparing 1-(6-methylpyridin-3-yl)-2-[4-(methylsulfonyl)phenyl]ethanone, an intermediate of etoricoxib
发明人:CASTELLIN ANDREA; STABILE PAOLO; FONTANA FRANCESCO; DE LUCCHI OTTORINO; CAPORALE ANDREA; TARTAGGIA STEFANO
权利人:CASTELLIN ANDREA; STABILE PAOLO; FONTANA FRANCESCO; DE LUCCHI OTTORINO; CAPORALE ANDREA; TARTAGGIA STEFANO; ITALIANA SINT SPA
摘要:A process for preparing 1-(6-methylpyridin-3-yl)-2-[4-(methyl sulfonyl)phenyl]ethanone, an intermediate of the synthesis of Etoricoxib. The synthesis of the intermediates useful for such preparation is also described.

专利号:US-2002165398-A1
优先权日:1998-03-12
标题:Modulators of protein tyrosine phosphatases (PTPases)
发明人:JEPPESEN LONE; ANDERSEN HENRIK SUNE; OLSEN OLE HVILSTED; JUDGE LUKE MILBURN; HOLSWORTH DANIEL DALE; BAKIR FARID; AXE FRANK URBAN; GE YU
摘要:The present invention provides novel compounds, novel compositions, methods of their use, and methods of their manufacture, where such compounds are pharmacologically useful inhibitors of Protein Tyrosine Phosphatases (PTPase's) such as PTP1B, CD45, SHP-1, SHP-2, PTPα, LAR and HePTP or the like. n The compounds are useful in the treatment of type I diabetes, type II diabetes, impaired glucose tolerance, insulin resistance, obesity, immune dysfunctions including autoimmunity diseases with dysfunctions of the coagulation system, allergic diseases including asthma, osteoporosis, proliferative disorders including cancer and psoriasis, diseases with decreased or increased synthesis or effects of growth hormone, diseases with decreased or increased synthesis of hormones or cytokines that regulate the release of/or response to growth hormone, diseases of the brain including Alzheimers disease and schizophrenia, and infectious diseases.

专利号:US-9566564-B2
优先权日:2014-02-07
标题 :Methodology for the formation of an extractive agent of polymerized carbon nanotubes encapsulating phenol nanoparticles used for DNA extraction and purification, and product thereof
发明人:SARLAK NAHID; JAFARI SAYYED MOSTAFA
权利人:SARLAK NAHID; JAFARI SAYYED MOSTAFA
摘要:A method for synthesis of nanocomposites using polymerized carbon nanotubes and phenolic compounds, such as 2,4-dichlorophenol, 4-nitrophenol, 2-nitrophenol, 4-chlorophenol, 2,4,6-trinitrophenol and phenol, in aqueous media, as well as the application of one of such nanocomposites, namely MWCNT-g-PCA-Phenol, as a DNA extraction agent. The aforementioned nanocomposites enable the isolation of genomic DNA of plant samples. Pursuant to the present invention, the toxicity of free phenols used in DNA extraction is decreased since very low concentrations of phenol are required in the method, as compared to conventional techniques which employ saturated phenol solutions. This remarkable advantage is due to the encapsulation of the phenol nanoparticles into the polymerized carbon nanotubes.

专利号:US-2002128496-A1
优先权日:2001-01-12
标题 :Process for the preparation of matrix metalloproteinase inhibitors
发明人:CHANG SOU-JENG; FERNANDO DILINIE P; GUPTA ASHOK; HILL DAVID R; WITTENBERGER STEVEN J
摘要:The present invention discloses a process for the synthesis of reverse hydroxamate matrix metalloproteinase (MMP) inhibitors.
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主要参考文献

[参考文献]: Daniel Tordera, Et Al. Efficient Green-Light-Emitting Electrochemical Cells Based On Ionic Iridium Complexes With Sulfone-Containing Cyclometalating Ligands. Chemistry. 2013 Jun 24;19(26):8597-609.
[参考文献]: I T Barnish, Et Al. Cerebrovasodilatation Through Selective Inhibition Of The Enzyme Carbonic Anhydrase. 3. 5-(Arylthio)-, 5-(Arylsulfinyl)-, And 5-(Arylsulfonyl)Thiophene-2-Sulfonamides. J Med Chem. 1981 Aug;24(8):959-64.

合成参考文献


摘要:Amatore, M.; Aubert, C.; Malacria, M.; Petit, M., Science of Synthesis Knowledge Updates, (2012) 3, 68.
摘要:Ipaktschi, J.; Saidi, M. R., Science of Synthesis Knowledge Updates, (2011) 3, 486.
摘要:Littke, A., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 1, 204.
摘要:Hay, M. B.; Hicks, J. D., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 2, 135.
摘要:Kelly, C. B.; Matsui, J. K.; Phelan, J. P.; Gutiérrez Bonet, Á.; Lang, S. B.; Molander, G. A., Science of Synthesis: Photocatalysis in Organic Synthesis, (2018) 1, 345.
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