CAS: 2113-68-0; [1,1'-Biphenyl]-4-Sulfonic Acid

该化合物是一种有机化合物,其特征是:在准位置上有一个联苯结构,代之以一个全氟辛烷磺酸组;该化合物一般是白色至浅黄色固体,由于极地磺酸功能组而溶于水中;该化合物具有酸性,在各种化学反应和应用中,包括作为有机合成的试剂和pH指标,具有实用性;该全氟辛烷磺酸组加强了它的再活动,使其得以参与电子药用替代反应;此外,[1,1欧元-双苯]-4-硫酸可以在不同工业过程中用作表面活性剂或分解剂;在正常条件下其稳定性及其在形成盐类和碱上的能力进一步有助于其在化学应用中的用途;在处理该化合物时,应注意安全防范措施,因为可能具有刺激性,因此许多磺酸.

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CAS号92-52-4 联苯 | CAS号98-80-6 苯硼酸 | CAS号19813-90-2 联苯-4-硫醇 | CAS号92-69-3 4-苯基苯酚 | CAS号2051-62-9 4-氯联苯 | CAS号1623-93-4 对联苯磺酰氯

合成工艺路线路线简述

    📜联苯置于氯磺酸体系中,用 氯仿 用作溶剂,化学反应生成联苯-4-磺酸
    参考文献:一系列有效的,系统可用的联苯磺酰胺基质金属蛋白酶抑制剂的结构活性关系和药代动力学分析.
    标题:一系列有效的,系统可用的联苯磺酰胺基质金属蛋白酶抑制剂的结构活性关系和药代动力学分析.
    摘要:制备了一系列(S)-2-(联苯基-4-磺酰基氨基)-3-甲基丁酸(5)的联苯磺酰胺衍生物,并评估了它们抑制基质金属蛋白酶(mmps)的能力.对于这一系列化合物,我们的目标是用结构上不同的功能性系统取代取代基上5的联苯和α-位置的取代基,以评估这些变化对生物学和药代动力学活性的影响.随后的结构活性关系(sar)研究表明,在4'-位(11C)处被溴取代的联苯磺酰胺显着提高了体外活性,并显示出优异的药代动力学(c(max),T(1/2),Aucs,相对于化合物5而言,可以通过用各种取代基取代11C的异丙基来改变α位的亲脂性,一般而言,与mmp-2,-3和-13相比,药效保持不变,但口服系统利用率较低.随后对其对映异构体11C'的评估表明,两种化合物都是同等有效的mmp抑制剂.相反,相应的异羟肟酸对映体对16A(s-异构体)和16A'(r-异构体)立体选择性抑制了mmp.在该系列中,16A'首次提
    Doi:10.1021/jm9903141

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    专利信息


    专利号:WO-2024126092-A1
    优先权日:2022-12-14
    标题:Method for producing 5-hmf by converting a syrup in a non-aqueous solvent with extraction of the syrup water upstream of the synthesis
    发明人:BOURAS MERIEM; DANG THI BICH NGOC; FERNANDEZ ESPADA PASTOR MARIA; LORCET HÉLÈNE; PAGOT ALEXANDRE; BREUIL PIERRE-ALAIN
    权利人:IFP ENERGIES NOW
    摘要:The present invention relates to a method for producing a 5-hydroxymethylfurfural (5-HMF) solution, comprising a step a) of bringing a feedstock comprising a hexose into contact with a synthesis solvent and an acid dehydration catalyst, said step being performed at a temperature of between 30 and 200°C, preferably between 50 and 180°C, more preferably between 70 and 150°C and very preferably between 90 and 130°C, and at a pressure of between 0.001 MPa and 10 MPa, preferably between 0.001 MPa and 5 MPa, more preferably between 0.01 MPa and 1 MPa, obtaining a reaction medium and concomitantly extracting the water from the reaction medium, in order to obtain a synthesis effluent comprising 5-HMF and synthesis solvent.

    专利号:WO-2025087830-A1
    优先权日:2023-10-25
    标 题:Production of 5-hmf in a non-aqueous solvent, with concentration of the 5-hmf prior to liquid-liquid extraction
    发明人:JACQUIN MARC; PAGOT ALEXANDRE
    权利人:IFP ENERGIES NOW
    摘要:The invention relates to a process for producing 5-hydroxymethylfurfural (5-HMF), comprising, in succession: a) bringing a sugar feedstock into contact with a polar aprotic synthesis solvent and an acid dehydration catalyst, at a temperature of 30-200°C and a pressure of 0.001-10 MPa, in order to produce a synthesis effluent that includes 5-HMF; b) concentrating the 5-HMF in the synthesis effluent; c) bringing the concentrated synthesis effluent into contact with an aqueous stream; d) liquid-liquid extraction with an organic extraction solvent, followed by a step e) of backwashing with an aqueous solvent in order to obtain an organic raffinate rich in 5-HMF and in solvent. The optionally concentrated organic raffinate is then subjected to a purification step g), for example hydrodistillation or crystallisation, in order to obtain a 5-HMF stream, for example in the form of an aqueous 5-HMF solution or crystalline 5-HMF.

    专利号:WO-2024126091-A1
    优先权日:2022-12-14
    标 题:Method for producing 5-hmf via conversion of sugar in a non-aqueous solvent with water extraction during synthesis
    发明人:BOURAS MERIEM; DANG THI BICH NGOC; FERNANDEZ ESPADA PASTOR MARIA; LARMIER KIM; LORCET HÉLÈNE; PAGOT ALEXANDRE
    权利人:IFP ENERGIES NOW
    摘要:The present invention relates to a method for producing a solution of 5-hydroxymethylfurfural (5-HMF), the method comprising a step a) of bringing a feedstock comprising a hexose into contact with a synthesis solvent and a dehydration acid catalyst, carried out at a temperature of between 30 and 200°C, preferably between 50 and 180°C, more preferably between 70 and 150°C and very preferably between 90 and 130°C, and at a pressure of between 0.001 MPa and 10 MPa, preferably between 0.001 MPa and 5 MPa, and more preferably between 0.01 MPa and 1 MPa, obtaining a reaction medium and concomitantly extracting the water from the reaction medium, to obtain a synthesis effluent comprising 5-HMF and synthesis solvent.

    专利号:WO-2023232427-A1
    优先权日:2022-05-31
    标 题:Synthesis of levulinic acid by hydration of furfuryl alcohol in the presence of a homogeneous acid catalyst and of a solvent based on ether and/or acetals

    专利号:EP-1957644-B1
    优先权日:2005-12-01
    标 题 :Enzymatic encoding methods for efficient synthesis of large libraries

    专利号:US-3442857-A
    优先权日:1965-11-10
    标题 :Boron trifluoride-hydrogen fluoride catalyzed synthesis of poly(aromatic sulfone) and poly(aromatic ketone) polymers
    发明人:THORNTON ROGER L
    权利人:DU PONT

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    合成参考文献


    参考文献:10.1107/s2059798324006557
    摘要:Dalwani S, Metz A, Huschmann FU, Weiss MS, Wierenga RK, Venkatesan R. Crystallographic fragment-binding studies of the Mycobacterium tuberculosis trifunctional enzyme suggest binding pockets for the tails of the acyl-CoA substrates at its active sites and a potential substrate-channeling path between them. Acta Crystallogr D Struct Biol. 2024 Jul 16;80(8):605–19. doi: 10.1107/s2059798324006557.
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