CAS: 634-91-3; 3,4,5-Trichloroaniline

该化合物是一种卤化阴性衍生物,配有分子式C6H2Cl3NH2.该化合物的特点是在芳香环上有三个氯替代成分,在各种化学条件下增强了其回活动性和稳定性.它是一个有机合成的多用途中间体,特别是在生产农用化学,染料和药品方面.氯原子的电子提取效应使它成为进一步功能化的宝贵建筑块.它的高度纯度和一贯质量确保工业应用的可靠性能.由于它潜在的毒性和环境影响,需要妥善处理.储存应处于冷,干燥和通风良好的区域.

结构式图片

欧盟法规

ECHA物质ECHA物质C&L通报REACH预注册

上下游产品

3,4,5-trichloronitrobenzen 5-bromo-1,2,3-trichloro-benzene N-(3,4,5-trichlorophenyl)acetamide 1-(3,4,5-trichloro-phenyl)-biguanide; hydr°Chloride N-(3,4-dichloro-phenyl)-N'-(3,4,5-trichloro-phenyl)-ureaN-(3,4-dichloro-phenyl)-N'-(3,4,5-trichloro-phenyl)-urea N,N'-bis-(3,4,5-trichloro-phenyl)-ureaN,N'-bis-(3,4,5-trichloro-phenyl)-urea

合成工艺路线路线简述

    📜1,2,3-三氯-5-硝基苯置于potassium Formate,Potassium Carbonate,异丙醇体系中,用46 %的收率获得产物3,4,5-三氯苯胺
    参考文献:从血红蛋白到单中心加氢催化剂
    标题:从血红蛋白到单中心加氢催化剂
    摘要:铁基单中心催化剂在实现高选择性化学过程方面具有巨大潜力,另外铁是一种富含地球的金属.它们在氧还原的电催化中被广泛探索,并在有机转化中显示出有前景的催化活性.特别是,Fen X @c 催化剂对于将硝基芳烃还原为芳香胺具有活性.然而,它们难以大规模生产,并且大多数制备方法都无法避免单点聚集.在这里,我们通过简单的两步过程从生物衍生化合物木糖和血红蛋白中制备了 Fen X @c 催化剂.由于血红蛋白天然含有 Fen X单中心,我们成功地将它们重新用于加氢催化中心,并在材料制备过程中避免了它们的聚集.通过像差校正透射电子显微镜和 X 射线吸收技术证明了它们的单点性质.它们被证明在将硝基芳烃转移氢化成苯胺方面具有活性,具有优异的底物选择性和可回收性,这在七个催化循环中保持的产率证明了这一点.我们还表明,Fen X @c 可用于通过还原/缩合串联制备 2-苯基苯并咪唑.我们的工作首次展示了生物质前体制备
    DOI:10.1039/d2Gc02344J

    海关参考信息

    专利信息


    专利号:US-5243032-A
    优先权日:1989-06-22
    标题:Preparation of azo pigments with low pcb content by coupling in the presence of olefins
    发明人:RIEPER WOLFGANG
    权利人:HOECHST AG
    摘要:The production which is customary in practice of monoazo compounds based on dichloro- and trichloroanilines or disazo compounds of the chlorinated biphenyl series by conventional coupling methods meets with difficulties in that the resulting pigments are contaminated by traces of polychlorinated biphenyls. n According to the invention, it has now been found that by addition of water-soluble olefins of the type ##STR1## (R =H, alk or Oalk; X =--COOR 1 , --CONHR 2 or --NR 3 COR 4 ) n in the azo coupling, the side reactions which form PCBs can be decidedly suppressed during synthesis of the pigments.

    专利号:US-5656742-A
    优先权日:1991-12-06
    标 题:Ring-opened purine compounds for labeling polynucleotides
    发明人:MCCABE MEAD M
    权利人:UNIV MIAMI
    摘要:The invention provides methods for attaching detectable labels to the N 7 -formyl group, of imidazole ring-opened alkylated purines and purine derivatives, directly, through a linking group, or by subsequent derivatization of a blocking group. The invention provides simple and efficient methods for labeling polynucleotides. In addition, the invention provides derivatized ring-opened alkylated purines and purine derivatives, including reagents for chemical and enzymatic synthesis of detectably labeled polynucleotides.

    专利号:US-4411912-A
    优先权日:1978-02-16
    标 题 :Insecticidal isovaleric acid esters
    发明人:HENRICK CLIVE A; GARCIA BARBARA A
    权利人:ZOECON CORP
    摘要:Esters and thiolesters of amino acids, intermediates therefor, synthesis thereof, and the use of said esters and thiolesters and compositions for the control of pests.

    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

    主要参考文献

    [参考文献]: D G Craciunescu, Et Al. On The Synthesis, Cytostatic And Antitumor Properties Of New Pt(Ii) And Pt(Iv) Complexes With Chloroanilines. Chem Biol Interact. 1985 Feb-Apr;53(1-2):45-56.

    合成参考文献


    参考文献:10.1016/j.chroma.2011.06.072
    摘要:Schubert J, Kappenstein O, Luch A, Schulz TG. Analysis of primary aromatic amines in the mainstream waterpipe smoke using liquid chromatography-electrospray ionization tandem mass spectrometry. J Chromatogr A. 2011 Aug 19;1218(33):5628–37. doi: 10.1016/j.chroma.2011.06.072.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知