CAS: 68449-30-9; 5-Bromo-3,4-Dihydronaphthalen-1(2H)-One

该化合物是一种有机化合物,其结构特征包括一个溴原子和一个与四龙框架相连的氯酮功能组;分子式一般反映碳,氢和溴原子的存在,表明其分类为卤化芳香化合物;该物质因其在有机合成中的潜在应用而闻名,特别是在制药和农用化学品开发中的潜在应用而闻名;溴的替代成分可增强再活性,使其在各种化学反应中有用,例如核糖核替代或合用反应;此外,氯酮组的存在有助于其再活动,并影响其物理特性,例如溶性和沸点;与许多溴化化合物一样,5-Bromo-1-troon可能展示具体的生物活动,这可能会引起对医药化学的兴趣;由于溴化化合物的潜在危害,包括毒性和环境影响,安全和处理预防措施至关重要.

结构式图片

欧盟法规

ECHA物质C&L通报

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3,4-二氢-1(2H)-萘酮 3,4-Dihydronaphthalene-1(2H)-One 529-34-0

合成工艺路线路线简述

    邻溴氰苄置于氢氧化钾,Lithium Aluminium Tetrahydride,三氯化铝,氯化亚砜,硫酸,氢溴酸,Sodium Ethanolate体系中,用 二硫化碳,乙醚,乙醇,水 作为反应溶剂,化学反应 24.75H,反应生成 5-溴-1-四氢萘酮
    参考文献:Synthesis Of Biological Markers In Fossil Fuels. 2. Synthesis And Carbon-13 NMR Studies Of Substituted Indans And Tetralins
    标题:Synthesis Of Biological Markers In Fossil Fuels. 2. Synthesis And Carbon-13 NMR Studies Of Substituted Indans And Tetralins
    摘要:
    DOI:10.1021/jo00196A024

    海关参考信息

    专利信息


    专利号:US-4777257-A
    优先权日:1983-08-25
    标题:Certain tetrahydronaphthyl or indanylcarboxylates and derivatives thereof which inhibit the synthesis of thromboxane
    发明人:KANAO MUNEFUMI
    权利人:DAIICHI SEIYAKU CO
    摘要:Benzocycloalkane derivatives of the formula (I) ##STR1## wherein: Z represents a methylene group or an ethylene group, either one of R 1 and R 2 represents --(CH 2 ) m --COOR 3 and the other represents ##STR2## wherein R 3 represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms, n represents an interger of 1 to 6 and m represents an interger of 0 to 5, and the physiologically acceptable salts thereof; having a strong and selective inhibition activity of thromboxane A 2 synthesis.

    专利号:US-9394264-B2
    优先权日:2009-11-13
    标 题:Sphingosine 1 phosphate receptor modulators and methods of chiral synthesis
    发明人:MARTINBOROUGH ESTHER; BOEHM MARCUS F; YEAGER ADAM RICHARD; TAMIYA JUNKO; HUANG LIMING; BRAHMACHARY ENUGURTHI; MOORJANI MANISHA
    权利人:RECEPTOS INC
    摘要:Compounds that selectively modulate the sphingosine 1 phosphate receptor are provided including compounds which modulate subtype 1 of the S1P receptor. Methods of chiral synthesis of such compounds are provided. Uses, methods of treatment or prevention and methods of preparing inventive compositions including inventive compounds are provided in connection with the treatment or prevention of diseases, malconditions, and disorders for which modulation of the sphingosine 1 phosphate receptor is medically indicated.

    专利号:US-9481659-B2
    优先权日:2011-05-13
    标 题 :Selective heterocyclic sphingosine 1 phosphate receptor modulators
    发明人:BOEHM MARCUS F; MARTINBOROUGH ESTHER; BRAHMACHARY ENUGURTHI; MOORJANI MANISHA; TAMIYA JUNKO; HUANG LIMING; YEAGER ADAM RICHARD
    权利人:BOEHM MARCUS F; MARTINBOROUGH ESTHER; BRAHMACHARY ENUGURTHI; MOORJANI MANISHA; TAMIYA JUNKO; HUANG LIMING; YEAGER ADAM RICHARD; CELGENE INT II SÀRL
    摘要:Compounds that selectively modulate the sphingosine 1 phosphate receptor are provided including compounds which modulate subtype 1 of the S1P receptor. Methods of chiral synthesis of such compounds is provided. Uses, methods of treatment or prevention and methods of preparing inventive compositions including inventive compounds are provided in connection with the treatment or prevention of diseases, malconditions, and disorders for which modulation of the sphingosine 1 phosphate receptor is medically indicated.

    专利号:US-8148370-B2
    优先权日:2008-03-21
    标题 :Polysubstituted derivatives of 2-aryl-6-phenyl-imidazo[1,2-a]pyridines, and preparation and therapeutic use thereof
    发明人:DE PERETTI DANIELLE; EVANNO YANNICK
    权利人:DE PERETTI DANIELLE; EVANNO YANNICK; SANOFI AVENTIS
    摘要:Compounds of formula (I): n nwherein R 1 , R 2 , R 3 , R 4 and X are as defined in the disclosure, or an acid addition salt thereof, and the therapeutic use and process of synthesis thereof.

    专利号:CA-2780433-C
    优先权日:2009-11-13
    标 题 :Sphingosine 1 phosphate receptor modulators and methods of chiral synthesis

    专利号:US-2015299150-A1
    优先权日:2009-11-13
    标题:Sphingosine 1 phosphate receptor modulators and methods of chiral synthesis
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    合成参考文献


    摘要:Thomas, A. W., Science of Synthesis, (2007) 31, 389.
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