CAS: 6996-92-5; Benzeneseleninicacid

该化合物是一种有机环化合物,其特征是:存在一个原子,结为苯环和酸性功能组;该化合物一般是白色的,光黄色固体,因其独特的化学特性而闻名,包括其作为核素的能力及其在有机合成中的潜在用途;二极溶剂中含有苯经乳酸,可溶解,便于其在各种化学反应中发生反应;在合成含有的化合物时经常使用,并可用作有机化学的试剂,特别是在形成银酸酯和其他衍生物时;此外,其含量具有独特的生物特性,使其对医药化学和研究中与在生物系统中的作用有关联,因此有必要谨慎处理该化合物,因为与化合物有关的潜在毒性.

结构式图片

欧盟法规

ECHA物质ECHA物质C&L通报REACH预注册

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合成工艺路线路线简述

    Benzeneseleninyl Chloride 反应生成 苯亚硒酸
    参考文献:401.臭氧对有机硒化合物的氧化
    标题:401.臭氧对有机硒化合物的氧化
    摘要:
    DOI:10.1039/jr9620002089

    海关参考信息

    专利信息


    专利号:US-5654441-A
    优先权日:1995-09-14
    标 题 :Synthesis of 1,3-oxathiolane sulfoxide compounds
    发明人:MCPHEE DEREK JAMES
    权利人:UNIROYAL CHEMICAL LTD
    摘要:A process for the production of a 1,3-oxathiolane sulfoxide of the formula ##STR1## wherein X is an amino group of the formula --NHR, wherein R is hydrogen, phenyl, C 1 -C 8 alkyl, C 3 -C 6 cycloalkyl, nitrophenyl, (C 1 -C 4 alkoxy)phenyl, furfuryl, halophenyl, tolyl, napthyl, biphenyl or hydroxyphenyl; or X is an alkoxy group of the formula --OR 1 wherein R is C 1 -C 6 alkyl, n which process comprises oxidizing a 1,3-oxathiolane of the formula ##STR2## wherein X is as defined above, in the presence of an effective amount of aqueous hydrogen peroxide and a sterically-hindered organoselenium compound of the formula ##STR3## wherein R 2 is aryl, mono-, di- or tri-substituted with C 1 -C 3 alkyl, n to the produce the 1,3-oxathiolane sulfoxide. This process stereoselectively produces the cis stereoisomer of the 1,3-oxathiolane sulfoxide. Additionally, there is disclosed a novel method for the preparation of 5,6-dihydro-2-methyl-1,4-oxathiin compounds using this process.

    专利号:US-5506223-A
    优先权日:1990-08-29
    标 题:Δ5-androstenes useful for promoting weight maintenance or weight loss and treatment process
    发明人:LARDY HENRY A; REICH IEVA L; WEI YONG
    权利人:HUMANETICS CORP
    摘要:A method for promoting weight control by treating a subject with a therapeutic amount of one of the DELTA 5-androstenes listed below to stimulate weight control without affecting appetite or inducing the synthesis of sex hormones. DELTA 5-Androstenes providing the desired biological activities include: DELTA 5-Androstene-3 beta ,7 alpha -diol-17-one (1) DELTA 5-Androstene-3 beta -ol-7,17-dione (2) DELTA 5-Androstene-3 beta ,7 alpha ,17 beta -triol (3) DELTA 5-Androstene-3 beta ,17 beta -diol-7-one (4) DELTA 5-Androstene-3 beta -acetoxy-7,16,17-trione (5) DELTA 5-Androstene-3 beta ,16 alpha -dihydroxy-7,17-dione (6) DELTA 5-Androstene-3 beta -propionoxy-16 beta -acetoxy-7,17-dione (7) DELTA 5-Androstene-3 beta ,7 alpha ,17 beta -triol-16-one (8) DELTA 5-Androstene-3 beta ,17 beta -diol-7,16-dione (9) DELTA 5-Androstene-3 beta ,16 alpha ,17 beta -triol-7-one (10) and derivatives thereof wherein one or more of the hydroxyl or keto substituents is a group convertible thereto by hydrolysis.

    专利号:JP-H09501153-A
    优先权日:1993-07-20
    标题 :Synthesis of taxol and its derivatives

    专利号:EP-0666746-B1
    优先权日:1993-09-02
    标题:$g(D)5-ANDROSTENES USEFUL FOR PROMOTING WEIGHT MAINTENANCE OR WEIGHT LOSS AND TREATMENT PROCESS
    发明人:LARDY HENRY A; REICH IEVA L; YONG WEI
    权利人:HUMANETICS CORP
    摘要:A method for promoting weight control by treating a subject with a therapeutic amount of one of the DELTA 5-androstenes listed below to stimulate weight control without affecting appetite or inducing the synthesis of sex hormones. DELTA 5-Androstenes providing the desired biological activities include: (1) DELTA 5-Androstene-3 beta ,7 alpha -diol-17-one, (2) DELTA 5-Androstene-3 beta -ol-7,17-dione, (3) DELTA 5-Androstene-3 beta ,7 alpha ,17 beta -triol, (4) DELTA 5-Androstene-3 beta ,17 beta -diol-7-one, (5) DELTA 5-Androstene-3 beta -acetoxy-7,16,17-trione, (6) DELTA 5-Androstene-3 beta ,16 alpha -dihydroxy-7,17-dione, (7) DELTA 5-Androstene-3 beta -propionoxy-16 beta -acetoxy-7,17-dione, (8) DELTA 5-Androstene-3 beta ,7 alpha ,17 beta -triol-16-one, (9) DELTA 5-Androstene-3 beta ,17 beta -diol-7,16-dione, (10) DELTA 5-Androstene-3 beta ,16 alpha ,17 beta -triol-7-one and derivatives thereof wherein one or more of the hydroxyl or keto substituents is a group convertible thereto by hydrolysis.

    专利号:GB-2165544-A
    优先权日:1984-10-16
    标题 :Synthesis of 20-keto-pregnanes via novel steroid 23-oxazolines

    专利号:CA-2183714-C
    优先权日:1995-09-14
    标 题:Synthesis of 1,3-oxathiolane sulfoxide compounds
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    主要参考文献


    1: Sands KN, Mendoza Rengifo E, George GN, Pickering IJ, Gelfand BS, Back TG. The Unexpected Role of SeVI Species in Epoxidations with Benzeneseleninic Acid and Hydrogen Peroxide. Angew Chem Int Ed Engl. 2020 Mar 9;59(11):4283-4287. doi: 10.1002/anie.201913566. Epub 2020 Jan 30.
    2: Palomba M, De Monte E, Mambrini A, Bagnoli L, Santi C, Marini F. A three- component [3 + 2]-cycloaddition/elimination cascade for the synthesis of spirooxindole-pyrrolizines. Org Biomol Chem. 2021 Jan 28;19(3):667-676. doi: 10.1039/d0ob02321c. 104(1):1-8. doi: 10.1016/j.jinorgbio.2009.09.007. Epub 2009 Sep 30. 23(3):1518-22. doi: 10.1021/la061727p. 55(2):210-23. doi: 10.1207/s15327914nc5502_13. 43(19):5919-30. doi: 10.1021/ic0494049. 56 (Pt 6):1029-34. doi: 10.1107/s0108768100010697. 96(5):1910-4. doi: 10.1073/pnas.96.5.1910.
    9: Zheng S, Xu P. [Synthesis of substituted benzeneseleninic acid and its antineoplastic activity]. Hua Xi Yi Ke Da Xue Xue Bao. 1995 Dec;26(4):371-4. Chinese.

    合成参考文献


    摘要:Jie, X.; Su, W., Science of Synthesis, (2022) , 45.
    摘要:D. DeFilippo and F. Momicchioli, Tetrahedron 25, 5733 (1969).
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