CAS: 4253-89-8; 1,2-Diisopropyldisulfane

该化合物是一种有机硫化合物,其特点是分硫功能组同异丙基替代成分结合,通常用于有机合成,催化和作为生产特殊化学品的中间体.该化合物的主要优势包括作为含有硫的分子的多功能构件发挥作用,有助于在制药,农用化学品和材料科学方面的应用.其相对稳定的脱硫联系允许在合成途径有控制的再活动.由于它独特的硫化物气味特征,异丙基二硫化物还被用于口味和香味工业.由于它具有潜在的易燃性和在特定条件下的再活动,妥善处理是必不可少的.

结构式图片

相似化合物

110-06-5 5943-30-6 1518-72-5

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上下游产品

hexamethyl-[1,3,5]trithiane 2-iodo-propane N,N'-dimethylthioperoxydicarbamic acid toluene-4-sulfonic acid isopropyl ester2-propanesulfonic acid 2-propanethiol Propionamid ethyl-isopropyl-disulfane

合成工艺路线路线简述

    丙酮置于硫化氢体系中,80.0 °C,784.47 Mpa 条件下,反应生成 异丙基二硫醚
    参考文献:Gem-Dithiols1
    标题:Gem-Dithiols1
    摘要:
    DOI:10.1021/ja01136A004

    专利信息


    专利号:US-9982005-B2
    优先权日:2013-04-04
    标 题 :Macrolides and methods of their preparation and use
    发明人:MYERS ANDREW G; SEIPLE IAN BASS; ZHANG ZIYANG
    权利人:HARVARD COLLEGE
    摘要:Provided herein are methods of preparing macrolides by the coupling of an eastern and western half, followed by macrocyclization, to provide macrolides, including both known and novel macrolides. Intermediates in the synthesis of macrolides including the eastern and western halves are also provided. Pharmaceutical compositions and methods of treating infectious diseases and inflammatory conditions using the inventive macrolides are also provided. A general diastereoselective aldol methodology used in the synthesis of the western half is further provided.

    专利号:US-11466046-B2
    优先权日:2014-10-08
    标题 :14-membered ketolides and methods of their preparation and use
    发明人:MYERS ANDREW G; SEIPLE IAN BASS; ZHANG ZIYANG
    权利人:HARVARD COLLEGE
    摘要:Provided herein are methods of preparing new 14-membered ketolides via coupling of an eastern and western half moiety, followed by macrocyclization, and optional functionalization. Intermediates in the synthesis of these ketolides including the eastern and western halves are also provided. Pharmaceutical compositions and methods of treating infectious diseases and inflammatory conditions using these ketolides are also provided.

    专利号:US-6432294-B1
    优先权日:2000-12-14
    标题 :Electrochemical activation of organic disulfides for electrophilic substitution
    发明人:GLASS RICHARD S; JOUIKOV VIATCHESLAV V; BOJKOVA NINA V
    权利人:UNIV ARIZONA
    摘要:Electrochemical oxidation of organic disulfides is conducted in an electrolytic solution containing an arene (e.g., anthracene, acenaphthylene, phenanthrene), and depending on the arene used and/or the product desired, an organic base (e.g., pyridine) to effect the synthesis of organothiated products in good yields.

    专利号:CN-108779138-A
    优先权日:2015-09-28
    标题:Design and synthesis of nucleotides based on novel disulfide linkers for use as reversible terminators for DNA sequencing by synthesis

    专利号:US-12150934-B2
    优先权日:2016-11-30
    标 题 :Methods of using substituted pyrazole and pyrazole compounds and for treatment of hyperproliferative diseases
    发明人:SIDDIQUI ARSHAD M; CIBLAT STEPHANE; CONSTANTINEAU-FORGET LEA; GRAND-MAITRE CHANTAL; GUO XIANGYU; SRIVASTAVA SANJAY; SHIPPS GERALD W; COOPER ALAN B; OZA VIBHA; KOSTURA MATTHEW W; LUTHER MICHAEL; LEVINE JEDD
    权利人:BANTAM PHARMACEUTICAL LLC
    摘要:Disclosed are methods of treating hyperproliferative disorders such as cancer, methods of arresting the cell cycle in cancer cells, methods of inhibiting glutathione synthesis in cancer cells, and associated compounds for use and uses in medicaments. In certain embodiments, the methods, uses and compounds are provided with reference to compounds of the structural formula (I), in which X1, X2, Z1, Z2, the ring system denoted by “aâ€?, R1, L1, L2, Q, L3, R3, L4, R4, L5, and R5 are as described herein. In certain embodiments, compounds disclosed herein are especially active against cancers having a mutant KRAS gene.

    专利号:US-6207838-B1
    优先权日:1999-04-30
    标 题 :Electrochemically generated organothiating reagents and their use
    发明人:GLASS RICHARD S; JOUIKOV VIATCHESLAV V
    权利人:UNIV ARIZONA
    摘要:Electrolysis of organic disulfides in liquid sulfur dioxide is used to obtain organothiating agents, which can then be reacted with appropriate substrates to effect the synthesis of organothioaromatic compounds efficiently and in high yields. With appropriate phenolic compounds, regioselective substitution occurs in which para substitution greatly exceeds ortho substitution.
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    主要参考文献

    参考标题:Investigations On Gold‐catalyzed Thioalkyne Activation Toward Facile Synthesis Of Ketene Dithioacetals
    作者:Xiaohan Ye,Jin Wang,Shengtao Ding,Seyedmorteza Hosseyni,Lukasz Wojtas,Novruz G. Akhmedov,Xiaodong Shi |发布日期:2017.8.4
    摘要:From A Gold‐associated Thioketene Intermediate. Based On This Interesting Mechanistic Insight, A Gold(I)‐catalyzed Thioether Addition To Thioalkynes Was Developed As A Novel Approach To Prepare Ketene Dithioacetals With Good Yields And High Efficiency.

    合成参考文献


    摘要:Lattanzi, A., Science of Synthesis: Stereoselective Synthesis, (2011) 3, 976.
    摘要:Xu, H.; Dai, H.-X., Science of Synthesis: Special Topics, (2022) 1, 195.
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