CAS: 16950-06-4; Fluoroantimonic Acid

该化合物是在传统酸无效的碳氢化合物转化,异构化和对流方面.HSbF6由于对水和大多数有机材料的活跃性反应,通常被作为氢氟氢或二氧化硫的一种溶液处理,其应用范围扩大到专门的合成化学和材料科学,尽管由于其腐蚀性和危险性质,需要严格的处理防范.

结构式图片

相似化合物

16925-25-0 16893-92-8 26042-64-8

欧盟法规

ECHA物质ECHA物质C&L通报REACH预注册

合成工艺路线路线简述

    📜五氟化锑 反应生成氢六氟锑酸盐
    参考文献:Gmelin Handbuch Der Anorganischen Chemie,Gmelin Handbook: Sb: Mvol.B2,8.5,Page 405-408
    标题:Gmelin Handbuch Der Anorganischen Chemie,Gmelin Handbook: Sb: Mvol.B2,8.5,Page 405-408

    专利信息


    专利号:US-2023286918-A1
    优先权日:2020-07-02
    标 题:Manufacturing process for 3,5-dichloropicolinonitrile for synthesis of vadadustat
    发明人:JURKAUSKAS VALDAS; JUNG YOUNG CHUN; KWON TAESOO; KANNAN ARUNACHALAM; GONDI VIJAYA BHASKER
    权利人:AKEBIA THERAPEUTICS INC
    摘要:Disclosed herein are methods and processes of preparing vadadustat or a pharmaceutically acceptable salts thereof, and intermediates (e.g., a compound of Formula (I), (I-F), (II), or (IV), or a pharmaceutically acceptable salts thereof) useful for the synthesis of vadadustat.

    专利号:US-11629137-B2
    优先权日:2017-04-24
    标 题:Methods of manufacturing of niraparib
    发明人:STEWART ALISTAIR; TOTO ANTHONY JOSEPH; CHEN FRANK XING; WU GEORGE
    权利人:TESARO INC
    摘要:Disclosed herein are methods and processes of preparing niraparib and pharmaceutically acceptable salts thereof, and intermediates and their salts useful for the synthesis of niraparib.

    专利号:WO-0144184-A1
    优先权日:1999-12-16
    标题:Synthesis of indole-containing spla2 inhibitors
    发明人:MARTINELLI MICHAEL JOHN; SAWYER JASON SCOTT
    权利人:LILLY CO ELI; MARTINELLI MICHAEL JOHN; SAWYER JASON SCOTT
    摘要:A method of making a compound include reacting a compound represented by formula (I), with a base, to form the compound of formula (II); and where R1 is H, R10 or -C(O)R10; R2 is R20 -OR20, -SR20, -NR20R20' or -C(O)R20;R3, R4, R5, R6 and R7 are each individually H, halogen, R, -OR, -SR, -NRR', -C(O)R, -C(O)OR, -S(O)R or -S(O)2R; provided that at least one of R4 and R5 is not H; each R, R10 and R20 is individually alkyl, alkenyl, alkynyl, aryl or heterocyclic radical; each R' and R20' is individually H, alkyl, alkenyl, alkynyl, aryl or heterocyclic radical; and W is a trisubstituted phosphorous. The method provides an alternative route to indole-3-glyoxylamide compounds.

    专利号:US-4218403-A
    优先权日:1979-04-06
    标 题 :Synthesis of aromatic aldehydes
    发明人:VANDERPOOL STEVEN H
    权利人:TEXACO DEVELOPMENT CORP
    摘要:Covers a method for preparing a para-alkyl substituted phenyl aldehyde by reacting carbon monoxide and an alkyl mono-substituted benzene in presence of a tantalum, niobium or antimony pentafluoride-hydrogen fluoride catalyst.

    专利号:WO-0144185-A1
    优先权日:1999-12-16
    标题 :Carbon monoxide-based synthesis of spla2 inhibitors
    发明人:SAWYER JASON SCOTT
    权利人:LILLY CO ELI; SAWYER JASON SCOTT
    摘要:A method of making a compound, comprises reacting a compound represented by formula (I), with CO and a catalyst, to form the compound of formula (II); where formula (I) is and, formula (II) is and where R2 is selected from the group consisting of R20 -OR20, -SR20, -NR20R20'and -C(O)R20; R3, R4, R5, R6 and R7 are each individually selected from the group consisting of H, halogen, R, -OR, -SR, -NRR', -C(O)R, -C(O)OR, -S(O)R and -S(O)2R; provided that at least one of R4 and R5 is not H; each R and R20 is individually selected from the group consisting of alkyl, alkenyl, alkynyl, aryl and heterocyclic radical; and each R' and R20' is individually selected from the group consisting of H, alkyl, alkenyl, alkynyl, aryl and heterocyclic radical. The method provides an alternative route to indole-3-glyoxylamide compounds.

    专利号:US-5399695-A
    优先权日:1992-04-10
    标 题:Method for the synthesis of quaternary ammonium salts
    发明人:NAKANO SHINJI; MORIMOTO TAKAO; ENDO TAKESHI
    权利人:NIPPON PAINT CO LTD
    摘要:Provided is a convenient method for synthesizing quaternary ammonium salts which are useful as curing catalysts for one-part thermosetting resin compositions which maintain storage stability at room temperature. The ammonium salts are synthesized by direct reaction of a benzyl alcohol or a benzyl alkyl ether optionally having on the benzene ring and/or at α-position one or more substituent groups inert to the intended reaction, with a corresponding strong-acid salt of a tertiary amine.

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    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

    主要参考文献

    [参考文献]: Rolf Minkwitz, Et Al. Halogenated Carboxonium Salts: Preparation And Structural Analysis. Inorg Chem. 1999 Mar 8;38(5):844-847.

    合成参考文献


    摘要:L808: ATSDR - Agency for Toxic Substances and Disease Registry (1990). Toxicological profile for silver. U.S. Public Health Service in collaboration with U.S. Environmental Protection Agency (EPA). http://www.atsdr.cdc.gov/toxprofiles/tp.asp id=539&tid=97
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