CAS: 58593-78-5; 4-Chloro-1,3-Benzenedithiol

该化合物是一种有机化合物,其特点是存在一种苯环,代之以两种硫醇(-SH)组和一种氯原子.该化合物是氯苯和硫酚类中的成员,具有两种功能组的典型特性.在室内温度下,黄色固体是无色的,在有机溶液中是可溶的,但由于苯环的防水性质,溶解性有限.青醇组的存在具有再活性,允许有机合成中的潜在应用,特别是在形成解硫化物或协调化学中作为离子体.此外,氯子构成可以影响化合物的再活性和稳定性,使化学反应变得有用.在处理该化合物时,应当注意安全防范,因为硫醇可能不易腐烂,并可能对健康造成风险.

结构式图片

MSDS等安全信息

上下游产品

4-chloro-1,3-benzenedisulfonyl dichloride 4-chloro-1,3-phenylenediamine 1-chloro-2,4-bis-(2,2-dimethoxy-ethylsulfanyl)-benzene 1-chloro-2,4-bis-methylsulfanyl-benzene 1-Chloro-2,4-bis-trifluoromethylsulfanyl-benzene 5-[2-Chloro-5-(4-methoxycarbonyl-4-methyl-pentylsulfanyl)-phenylsulfanyl]-2,2-dimethyl-pentanoic acid methyl ester

合成工艺路线路线简述

    📜4-氯-1,3-苯二胺 反应生成 4-氯-1,3-苯二硫醇
    参考文献:Schaefer,Ted; Baleja,James D.; Penner,Glenn H.,Canadian Journal Of Chemistry,1985,Vol. 63,P. 2471-2475
    标题:Schaefer,Ted; Baleja,James D.; Penner,Glenn H.,Canadian Journal Of Chemistry,1985,Vol. 63,P. 2471-2475

    海关参考信息

    专利信息


    专利号:US-2009111737-A1
    优先权日:1999-05-24
    标题:Novel antibacterial agents
    发明人:CHRISTENSEN BURTON G; MORAN EDMUND J; GRIFFIN JOHN H; JUDICE J KEVIN; MU YONGQI; PACE JOHN L; MAMMEN MATHAI; AGGEN JAMES
    权利人:CHRISTENSEN BURTON G; MORAN EDMUND J; GRIFFIN JOHN H; JUDICE J KEVIN; MU YONGQI; PACE JOHN L; MAMMEN MATHAI; AGGEN JAMES
    摘要:This invention relates to novel multibinding compounds (agents) that are antibacterial agents. The multibinding compounds of the invention comprise from 2-10 ligands covalently connected by a linker or linkers, wherein each of said ligands in their monovalent (i.e., unlinked) state have the ability to bind to a an enzyme involved in cell wall biosynthesis and metabolism, a precursor used in the synthesis of the bacterial cell wall and/or the bacterial cell surface thereby interfere with the synthesis and/or metabolism of the cell wall. In particular the multibinding compounds of the invention comprise from 2-10 ligands covalently connected by a linker or linkers, wherein each of said ligands hasn a ligand domain capable of binding to penicillin binding proteins, a transpeptidase enzyme, a substrate of a transpeptidase enzyme, a beta-lactamase enzyme, pencillinase enzyme, cephalosporinase enzyme, a transglycoslase enzyme, or a transglycosylase enzyme substrate; Preferably, the ligands are selected from the beta lactam or glycopeptide class of antibacterial agents.

    专利号:US-7179794-B2
    优先权日:1998-06-08
    标题 :Multivalent macrolide antibiotics
    发明人:GRIFFIN JOHN H; PACE JOHN L
    权利人:THERAVANCE INC
    摘要:Disclosed are multibinding compounds which include macrolide antibiotics, aminoglycosides, lincosamides, oxazolidinones, streptoramins, tetracycline and/or other compounds which bind to bacterial ribosomal RNA and/or to one or more proteins involved in ribosomal protein synthesis in the bacterium, which are useful in treating bacterial infections. The compounds adversely affect protein expression and have an antibacterial effect. The multibinding compounds of this invention containing from 2 to 10 ligands covalently attached to one or more linkers. Each ligand is macrolide antibiotic, aminoglycoside, lincosamide, oxazolidinone, streptogramin, tetracycline or other compound which binds to bacterial ribosomal RNA and/or one or more proteins involved in ribosomal protein synthesis in the bacterium.

    供应商参考报价(招募中)

    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
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知