CAS: 719-22-2; 2,6-Di-Tert-Butylcyclohexa-2,5-Diene-1,4-Dione

该化合物是一种有分立障碍的五角星衍生物,其特点是其强力氧化稳定性和电子接受特性.三丁基替代物增强了抗降解性,使之适合在氧化条件下需要长期稳定的应用.这种化合物通常用作有机合成的中间体,特别是在制备红氧化活性材料和作为聚合物化学稳定剂时.其硬性环己二二烯核心促进了控制电子转移过程,而散装三丁基组则尽量减少不必要的副反应.这些特征使它在精确氧化性转化至关重要的研究和工业环境中成为有价值的试剂.

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CAS号88-26-6 2,6-二叔丁基-4-羟甲基苯酚 | CAS号2444-28-2 2,6-二叔丁基-1,4-苯二酚 | CAS号128-39-2 2,6-二叔丁基苯酚 | CAS号489-01-0 2,6-二叔丁基-4-甲氧基苯酚 | CAS号14387-17-8 Benzenemethanol... | CAS号128-37-0 抗氧剂BHT | CAS号75498-73-6 2,6-di-tert-but... | CAS号2455-14-3 3,3',5,5'-四叔丁基-... | CAS号1620-98-0 3,5-二叔丁基-4-羟基苯甲醛 | CAS号1138-52-9 3,5-二叔丁基苯酚 | CAS号489-01-0 2,6-二叔丁基-4-甲氧基苯酚 | CAS号14329-20-5 2,6-ditert-buty... | CAS号950-58-3 4-氨基-2,6-二-叔丁基苯酚 | CAS号2444-24-8 Phenol,2,6-bis(... | CAS号128-39-2 2,6-二叔丁基苯酚 | CAS号2455-14-3 3,3',5,5'-四叔丁基-... | CAS号955-03-3 2,6-二-叔丁基-4-亚硝基苯酚 | CAS号36384-85-7 PHENOL, 2,6-BIS... | CAS号34959-61-0 4-(dichlorometh... | CAS号36384-88-0 2,6-ditert-buty...

合成工艺路线路线简述

  • 6386-38-5 = 719-22-2 + 131692-75-6 + 82304-66-3
    反应条件:1.1 Catalysts: Vanadate(6-),Nona-μ-Oxotrioxo(Pentadeca-μ-Oxononaoxononamolybdate)[μ12-[phospha... Solvents: Methanol
    标题:Catalytic Oxidation Of 4-Oxoalkyl-Substituted 2,6-Di-Tert-Butylphenol In The Presence Of Trivanadium Molybdophosphoric Heteropolyacids
    作者:Titova,T. F.; Et Al
    参考文献:Zhurnal Prikladnoi Khimii (Sankt-Peterburg 日期:1990 卷标:63(8) 页码:1761-5]

    6386-38-5 = 719-22-2 + 131692-74-5 + 82304-66-3
    反应条件:1.1 Catalysts: Vanadate(6-),Nona-μ-Oxotrioxo(Pentadeca-μ-Oxononaoxononamolybdate)[μ12-[phospha... Solvents: Benzene
    标题:Catalytic Oxidation Of 4-Oxoalkyl-Substituted 2,6-Di-Tert-Butylphenol In The Presence Of Trivanadium Molybdophosphoric Heteropolyacids
    作者:Titova,T. F.; Et Al
    参考文献:Zhurnal Prikladnoi Khimii (Sankt-Peterburg 日期:1990 卷标:63(8) 页码:1761-5
2,6-二叔丁基-4-甲基苯酚置于[cuii(η1-O2•−)(Tris(5-(2,4,6-Triphenylbenzene)-2-Pyridylmethyl)Amine)]+体系中,用 四氢呋喃 作为反应溶剂,以48%的收率获得产物2,6-二叔丁基苯醌
参考文献:空间稳定的末端超氧铜 (II) 配合物及其与 O-H,N-H 和 C-H 底物反应性的机理研究
标题:空间稳定的末端超氧铜 (II) 配合物及其与 O-H,N-H 和 C-H 底物反应性的机理研究
摘要:末端超氧铜 (II) 配合物在转化为过氧桥联二铜 (II) 配合物方面的不稳定性在很大程度上限制了他们在极低温度下的研究.这限制了它们氧化底物的动力学能力.作为回应,我们开发了一系列庞大的配体 Ar 3-Tmpa (Ar = Tpb,Dpb,Dtbpb),并使用它们来支持与 O 2反应反应生成[cu Ii (η 1-O 2 •-)(Ar 3-Tmpa)] +物质,在所有温度下对二聚化都是稳定的.o 2的结合在低于环境温度时饱和,并且可以通过变暖来逆转.ar = Tpb 和 Dpb 系统在 25 oc 时开始氧化,所有三种 [cu Ii (η 1-O 2 •-)(Ar 3-Tmpa)] +配合物在温度<=−20 oc.这为研究这些配合物提供了一个较宽的温度窗口,通过使用广泛的 O-H对 [cu Ii (η 1-O 2 •-)(Tpb 3-Tmpa)] +进行广泛的反应动力学测量来利用这一点,N-H
DOI:10.1021/jacs.1C07837

海关参考信息

专利信息


专利号:US-5527824-A
优先权日:1985-07-22
标题 :Substituted Di-T-Butlyphenols useful for inhibiting leukotriene synthesis
发明人:SCHERRER ROBERT A
权利人:RIKER LABORATORIES INC
摘要:Substituted Di-T-Butylphenols useful for inhibiting the synthesis of leukotrienes are disclosed.

专利号:US-3663578-A
优先权日:1969-10-18
标题 :Catalytic oxidation of alkyl-substituted hydroquinones to the corresponding p-benzoquinones
发明人:KUTEPOW NIKOLAUS VON; MAGIN AUGUST; JOSCHEK HANS-INGO
权利人:BASF AG
摘要:AIR OXIDATION OF ALKYL-SUBSTITUTED HYDROQUINONES IN THE PRESENCE OF HEAVY METAL SALTS AS CATALYSTS IN A LIQUID MIXED PHASE CONSISTING OF AN AQUEOUS PHASE AND AN ORGANIC PHASE. THE AQUEOUS PHASE CONTAINS DISSOLVED CATALYST AND ADDITIVES FOR SETTING UP A PH BELOW 7, AND THE ORGANIC PHASE IS A SELECTIVE SOLVENT FOR THE ALKYL-SUBSTITUTED PBENZOQUINONE FORMED IN THE OXIDATION. THE PROCESS ENABLES 2,3,6-TRIMETHYLHYDROQUINONE, AN IMPORTANT INTERMEDIATE IN THE SYNTHESIS OF VITMIN E, TO BE SEPARATED FROM MIXTURES OF METHYL-SUBSTITUTED HYDROQUINONES.

专利号:US-9309357-B2
优先权日:2013-06-18
标题:Synthesis of free radical polymerizable ethylenically unsaturated poloxamers and poloxamines
发明人:AWASTHI ALOK KUMAR; KUNZLER JAY F; SATYANARAYANA GANUGAPATI; RAI NOOJI SATHEESHA
权利人:BAUSCH & LOMB
摘要:A new synthetic method of forming free radical polymerizable end terminal functionalized poloxamers and poloxamines in commercial scale batches which uses a binary system of inhibitors to eliminate the formation of high molecular weight impurities. It has also been surprisingly discovered that the inorganic impurities formed during the commercial scale synthetic process are removed by the use of resin materials.

专利号:US-7368624-B2
优先权日:2004-03-30
标 题 :Synthesis for polycyclic aromatic hydrocarbon compounds
发明人:BROWN CHRISTOPHER T; SHUKLA DEEPAK; DOCKERY KEVIN P; LENHARD JEROME R; MATZ JAMES R
权利人:EASTMAN KODAK CO
摘要:A process for forming an aryl-aryl bond comprises the step of reacting an arene hydrocarbon compound with either (1) an organic oxidant selected from the group consisting of a quinone, a quinone imine, a quinone diimine, and a nitroarene, or (2) an oxidizing salt selected from the group consisting of a triarylaminium salt, an oxonium salt, and a nitrosium salt, or (3) a hypervalent iodine compound, each in the presence of a Brönsted or Lewis acid.

专利号:US-6118029-A
优先权日:1997-01-30
标题:Process for producing 3,3',5,5'-tetra-t butylbiphenol
发明人:ISOTA YOICHIRO; YAO KAZUHIKO; KAWAHARA MIKIO
权利人:HONSHU CHEMICAL IND
摘要:A batch or continuous process produces highly pure 3,3',5,5'-tetra-t-butylbiphenol suitable as a starting material for the synthesis of 4,4'-biphenol. The process for producing 3,3',5,5'-tetra-t-butylbiphenol comprises conducting an oxidation coupling of purified 2,6-di-t-butylphenol(i) or crude 2,6-di-t-butylbiphenol(ii), said crude 2,6-di-t-butylphenol being obtained by reacting isobutylene with phenol in the presence of an aluminum catalyst, and removing the aluminum catalyst. The 2,6-di-t-butylphenol is oxidatively coupled in an alkali metal catalyst mixture comprising (1) an alkali metal catalyst and alkylphenols, or (2) alkali metal catalyst, alkylphenols and phenol to produce 3,3',5,5'-tetra-t-butylbiphenol. The oxidative coupling is conducted together with 10-30% by weight of phenol and/or t-butylphenol per 100% by weight of 2,6-di-t-butylphenol in the presence of an alkali metal catalyst.

专利号:EP-3010946-A1
优先权日:2013-06-18
标 题:Synthesis of free radical polmerizable ethylenically unsaturated poloxamers and poloxamines
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主要参考文献

参考标题:Organophotocatalytic Aerobic Oxygenation Of Phenols In A Visible‐light Continuous‐flow Photoreactor
作者:Joël Wellauer,Dragan Miladinov,Thomas Buchholz,Jan Schütz,René T. Stemmler,Jonathan A. Medlock,Werner Bonrath,Christof Sparr |发布日期:2021.7.7
摘要:A Mild Photocatalytic Phenol Oxygenation Enabled By A Continuous-Flow Photoreactor Using Visible Light And Pressurized Air Is Described Herein. Products For Wide-Ranging Applications, Including The Synthesis Of Vitamins, Were Obtained In High Yields By Precisely Controlling Principal Process Parameters. The Reactor Design Permits Low Organophotocatalyst Loadings To Generate Singlet Oxygen. It Is Anticipated

合成参考文献


参考文献:10.1136/thx.2010.156695
摘要:Ibrahim B, Basanta M, Cadden P, Singh D, Douce D, Woodcock A, Fowler SJ. Non-invasive phenotyping using exhaled volatile organic compounds in asthma. Thorax. 2011 Sep;66(9):804–9. doi: 10.1136/thx.2010.156695.
参考文献:10.1007/s00216-011-5209-7
摘要:Chuang H, Jones T, Chen Y, Bell J, Wenger J, BéruBé K. Characterisation of airborne particles and associated organic components produced from incense burning. Analytical and Bioanalytical Chemistry. 2011 Jul 17;401(10):3095–102. doi: 10.1007/s00216-011-5209-7.
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