CAS: 617-97-0; 3-Methylbenzenesulfonic Acid

该化合物是一种有机磺酸衍生物,在有机合成和工业应用中广泛用作强酸催化剂,其主要优势包括极地溶剂中的高溶性,热稳定性和持续反应性,使之适合酯化,通融和聚合反应. 化合物的强酸性能和低挥发性增强了实验室和制造环境中的流程控制和安全. 此外,它作为多种药物,染料和表面活性剂的中间体. 它的晶体形式确保了处理和精确剂量的方便性,而它与各种反应条件的兼容性则凸显了它在各种化学工艺中的实用性.

结构式图片

欧盟法规

C&L通报

上下游产品

ethanol sodium ethanolate 5-methyl-2-diazobenzenesulphonic acid 3-methylbenzene diazoniumo-toluenesulfonic acid toluene-4-sulfonic acid toluene allyl 3-fluoro-5-nitrobenzoate

合成工艺路线路线简述

    📜3-甲基苯硫酚置于tetrakis(Pyridine)Silver(II) Peroxodisulfate体系中,用 乙腈 作为反应溶剂,化学反应 2.0H,以80%的收率获得产物3-甲基苯磺酸
    参考文献:Tetrakis(Pyridine)Silver(II) Peroxodisulfate,[ag(Py)4]S2O8,A Reagent For The Oxidative Transformations
    标题:Tetrakis(Pyridine)Silver(II) Peroxodisulfate,[ag(Py)4]S2O8,A Reagent For The Oxidative Transformations
    摘要:四吡啶合银(II)过氧二硫酸盐可将芳香醛氧化为羧酸,苄醇氧化为羰基化合物,芳香硫醇及烯丙基芳基硫醚氧化为芳磺酸,苄基碳-氢键氧化为羰基化合物.α-羟基羧酸和苯乙酸发生脱羧反应,反应生成羰基化合物.二苄醚及其硫类似物分别转化为相应的酯和硫酯.
    DOI:10.1246/bcsj.65.2878

    海关参考信息

    专利信息


    专利号:US-11858953-B2
    优先权日:2018-04-04
    标 题:Compositions and methods for synthesis of phosphorylated molecules
    发明人:CHAPUT JOHN; LIAO JEN-YU; BALA SAIKAT
    权利人:UNIV CALIFORNIA
    摘要:The invention provides compositions and methods for synthesis of phosphorylated organic compounds, including nucleoside triphosphates.

    专利号:US-8492390-B2
    优先权日:2002-05-08
    标题 :Synthesis of locked nucleic acid derivatives
    发明人:DETLEF SORENSEN MADS; WENGEL JESPER; KOCH TROELS; CHRISTENSEN SIGNE M; ROSENBOHM CHRISTOPH; PEDERSEN DANIEL SEJER
    权利人:DETLEF SORENSEN MADS; WENGEL JESPER; KOCH TROELS; CHRISTENSEN SIGNE M; ROSENBOHM CHRISTOPH; PEDERSEN DANIEL SEJER; SANTARIS PHARMA AS
    摘要:The invention relates to a novel strategy for the synthesis of Locked Nucleic Acid derivatives, such as α- L -oxy-LNA, amino-LNA, α- L -amino-LNA, thio-LNA, α- L -thio-LNA, seleno-LNA and methylene LNA, which provides scalable high yielding reactions utilising intermediates that also can produce other LNA analogues such as oxy-LNA. Also, the compounds of the formula X are important intermediates that may be reacted with varieties of nucleophiles leading to a wide variety of LNA analogues.

    专利号:EP-1501848-B1
    优先权日:2002-05-08
    标 题 :Synthesis of locked nucleic acid derivatives
    发明人:SORENSEN MADS DETLEF; WENGEL JESPER; KOCH TROELS; CHRISTENSEN SIGNE M; ROSENBOHM CHRISTOPH; PEDERSEN DANIEL SEJER
    权利人:SANTARIS PHARMA AS
    摘要:The invention relates to a novel strategy for the synthesis of Locked Nucleic Acid derivatives, such as alpha-L-oxy-LNA, amino-LNA, alpha-L-amino-LNA, thio-LNA, alpha-L-thio-LNA, seleno-LNA and methylene LNA, which provides scalable high yielding reactions utilising intermediates that also can produce other LNA analogues such as oxy-LNA. Also, the compounds of the formula X are important intermediates that may be reacted with varieties of nucleophiles leading to a wide variety of LNA analogues. (Formula I)

    专利号:US-9975866-B2
    优先权日:2013-11-21
    标 题:Process for synthesis of furan derivative using an acid catalyst and preparation thereof
    发明人:LALI ARVIND MALLINATH; PAWAR HITESH SURESH
    权利人:DEPARTMENT OF BIOTECH MINISTRY OF SCIENCE AND TECH GOVERNMENT OF INDIA; INSTITUTE OF CHEMICAL TECH; DEPARTMENT OF BIOTECH MINISTRY OF SCIENCE AND TECH GOVERNMENT OF INDIA
    摘要:In accordance with the present subject matter, there is provided a process for preparing a furan derivative, the process comprising the steps of contacting a sugar with a monophasic organic solvent to obtain a reaction mixture; and subjecting the reaction mixture to a temperature in the range from 100° C. to 180° C., in presence of an acid catalyst, for a time period in the range of 0.5 min to 4.0 h to obtain at least 70% conversion of the sugar to a single furan derivative, wherein the acid catalyst is selected from the group consisting of homogenous acid catalyst, heterogenous solid acid catalyst, and combinations thereof. There is also provided a process for preparation of a heterogenous solid acid catalyst.

    专利号:US-8329131-B2
    优先权日:2004-01-22
    标题:Isotopically-enriched boranes and methods of preparing them
    发明人:SPIELVOGEL BERNARD; COOK KEVIN S
    权利人:SPIELVOGEL BERNARD; COOK KEVIN S; SEMEQUIP INC
    摘要:The invention provides new methods for synthesis of large boron hydride clusters, e.g., boron hydride molecules of the formula B n H m where 5≦n≦96 and m≦n+8, wherein m and n satisfy the electron counting rules of macropolyhedral boranes. The invention is particularly useful for synthesis of octadecaborane (B 18 H 22 ). Preferred methods of the invention include iteratively generating a conjugate acid from a salt of the [B a H b ] c− or [B n+2 H m−4 ] 2− anion followed by degradation under conditions conducive to concentrating and drying of the conjugate acid to provide a borane B n H m and residual salt of the [B a H b ] c− or [B n+2 H m−4 ] 2− anion which is reused in the method of synthesis. The invention further provides isotopically enriched boranes, particularly isotopically enriched 10 B 18 H 22 and 11 B 18 H 22 .

    专利号:US-2018274001-A1
    优先权日:2017-03-21
    标 题 :Nucleic acid synthesis using dna polymerase theta
    发明人:EFCAVITCH J WILLIAM; TUBBS JULIE L
    权利人:MOLECULAR ASSEMBLIES INC
    摘要:Provided herein are methods for template-independent synthesis of oligonucleotides using a DNA polymerase. Also provided are methods for template-directed synthesis of oligonucleotides and for sequencing of nucleic acids using DNA polymerase theta and 3′-aminoalkoxy nucleotides.

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:Fravel, B.; Murugan, R.; Scriven, E. F. V., Science of Synthesis, (2007) 31, 757.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知