CAS: 32740-79-7; Ruthenium(Iv) Oxide Xhydrate

该化合物是一种无机化合物,其特征为深褐色至黑色外观,是一种水化的氧化亚氮,其酸盐处于+4氧化状态,以其高度稳定性著称,并常常用作各种化学反应的催化剂,特别是在燃料电池和电解等电化学应用中的催化剂;环氧水合物的表面半导体特性,并能够促进有机化合物的氧化.其结构通常由铁合亚原子组成,与氧协调,形成一个可吸收水分子的网络.该化合物在强酸中溶解溶,可通过各种方法合成,包括鲁泰亚盐的热分解.由于其独特的特性,它有可能用于材料科学,纳米技术和其他基于氨的化合物的前体.然而,处理应谨慎进行,因为许多金属氧化物与接触可能构成的健康风险,因此应对许多金属氧化物进行处理.

结构式图片

欧盟法规

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    专利信息


    专利号:US-2023183177-A1
    优先权日:2020-04-24
    标题:Enantioselective chemo-enzymatic synthesis of optically active amino amide compounds
    发明人:GRILL BIRGIT; WINKLER MARGIT; SCHWAB HELMUT; STROHMEIER GERNOT; DONSBACH KAI; WALDVOGEL SIEGFRIED R; ARNDT SEBASTIAN; WEIS DOMINIK
    权利人:PHARMAZELL GMBH
    摘要:The present invention relates to a novel biocatalytic process for the stereoselective preparation of alpha amino amide compounds catalyzed by NHase enzymes. A further aspect of the invention relates to novel NHase enzymes as well as further improved NHase enzyme mutants, nucleic acid molecules encoding these enzymes, recombinant microorganisms suitable for preparing such enzymes and mutants. Another aspect of the invention relates to a chemo-biocatalytic process for the preparation of lactam compounds comprising the new catalytic process for the preparation of alpha amino amide compounds catalyzed by NHase enzymes, as well as the chemical oxidation of the alpha amino amide by applying certain chemical oxidation catalysts suitable for converting the alpha amino amide under retention of its stereochemical configuration to the respective lactam. The novel chemo-biocatalytic process is particularly suited for the synthesis of valuable pharmaceutical compounds, like in particular (S)-Levetiracetam.

    专利号:US-5591867-A
    优先权日:1992-12-04
    标 题 :Synthesis of kainic acid
    发明人:MONN JAMES A
    权利人:LILLY CO ELI
    摘要:This invention provides a process for preparing kainic acid and provides intermediates in the synthesis thereof.

    专利号:US-2023303487-A1
    优先权日:2020-07-31
    标 题 :Process for preparation of mesotrione and its intermediates
    发明人:PANIRAJ A S; KUMAR SURESH D; S V R ADITHYA
    权利人:RALLIS INDIA LTD
    摘要:The present disclosure provides a new and improved process for preparation of intermediate compounds and synthesis of mesotrione therefrom. The present disclosure provides an economical, efficient and eco-friendly process for preparation of mesotrione.

    专利号:US-11512097-B2
    优先权日:2019-11-25
    标题 :Heterocyclic compounds as Delta-5 desaturase inhibitors and methods of use
    发明人:ALLEN JENNIFER R; BELTRANI MICHELA; BOURBEAU MATTHEW P; DAMYANOVA TEODORA P; LINGARD IAIN; MINATTI ANA E; VINCETTI PAOLO
    权利人:AMGEN INC
    摘要:The present disclosure provides compounds useful for the inhibition of Delta-5 Desaturase (“D5Dâ€?). The compounds have a general Formula I n nwherein the variables of Formula I are defined herein. This disclosure also provides pharmaceutical compositions comprising the compounds, uses of the compounds, and compositions for treatment of, for example, a metabolic or cardiovascular disorder. Further, the disclosure provides intermediates useful in the synthesis of compounds of Formula I.

    专利号:US-2014235840-A1
    优先权日:2011-09-30
    标 题:New synthesis of fucose
    发明人:KHANZHIN NIKOLAY; BOUTET JULIEN; BONACCORSI FILIPPO; DEKANY GYULA
    权利人:GLYCOM AS
    摘要:A process for converting D-glucose into L-fucose, where a first aspect of the disclosure relates to a method of making a compound of formula (1) wherein R is independently H, alkyl or phenyl or, preferably, wherein the two germinal R groups together with the carbon atom to which they are attached form a C3-s cycloalkylidene group, including the step of treating a compound of formula (2) wherein R is defined above and R 1 is a sulphonate leaving group, with a reducing complex metal hydride and, preferably, a base to form the compound of formula (1); a compound of formula (13).

    专利号:US-2024246990-A1
    优先权日:2019-10-14
    标 题:Process of preparing (1r, 4r, 5s)-4-(2-chloroethyl)-1-((s)-((s)-cyclohex-2-en-1-yl)(hydroxy)methyl)-5-methyl-6-oxa-2-azabicyclo[3.2.0]heptane-3,7-dione(salinosporamide a; marizomib)
    发明人:YONG KELVIN; TRAVERSE JOHN; GEHERTY MARYLL
    权利人:CELGENE INT II SARL
    摘要:The present invention is directed to a process for the synthesis of (1R, 4R, 5S)-4-(2-chloroethyl)-1-((S)-((S)-cyclohex-2-en-1-yl)(hydroxy)methyl)-5-methyl-6-oxa-2-azabicyclo[3.2.0]heptane-3,7-dione; compound 1 (salinosporamide A, marizomib):
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    合成参考文献


    参考文献:10.1007/s11426-022-1439-1
    摘要:Bao Z, Zhang Y, Wang L, Wu X. Difluoroalkylative carbonylation of alkenes to access carbonyl difluoro-containing heterocycles: convenient synthesis of gemigliptin. Sci. China Chem. 2022 Dec 12;66(1):139–46. doi: 10.1007/s11426-022-1439-1.
    参考文献:10.1007/s41403-023-00444-5
    摘要:Sivakumar V, Rao PG. Sonochemical Applications for Process Industries: A Comprehensive Analysis and Review. Trans Indian Natl. Acad. Eng. 2024 Feb 05;9(1):1–24. doi: 10.1007/s41403-023-00444-5.
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