CAS: 2025-95-8; 1,8-Bis(Bromomethyl)Naphthalene

该化合物是一种有机化合物,其特点是其氯化萘脊椎,在1和8个位置上有2个溴甲基组,该化合物在室内温度下一般是白色至光黄色固体,由于存在溴原子,可参与各种化学反应,包括核生殖替代,因此已知其具有反应性.该化合物经常被用作有机合成的中间体,特别是在准备更复杂的分子时.该溴甲基组的存在增强了其在交叉相交反应中的效用,并成为聚合工艺的建筑块.此外,1,8-双(溴甲基)甲型甲型六氯环己烷在有机溶剂中表现出中等溶性,适合各种实验室应用.在处理该化合物时,应采取安全防范措施,因为溴化化合物可能具有危险性,并可能对环境造成危害.适当的储存和处置方法对于减少与使用该化合物有关的潜在危害至关重要.

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naphthalene-1,8-diyldimethanol 1,8-Naphthalic anhydride 1,8-dimethylnaphthalene dimethyl naphthalene-1,8-dicarboxylate 1,8-dimethylnaphthalene acenaphthene 2,3-dihydro-(2-phenylmethyl)-1H-benz[de]isoquinoline -triphenylphosphoniumbromid8-Brommethylnaphthyl-(1)-methyl-triphenylphosphoniumbromid

合成工艺路线路线简述

    📜1,8-萘二甲酸二甲酯置于吡啶,Lithium Aluminium Tetrahydride,乙醚,三溴化磷,苯体系中,化学反应生成1,8-双(溴甲基)萘
    参考文献:A New Synthesis Of Acenaphthene
    标题:A New Synthesis Of Acenaphthene
    摘要:
    Doi:10.1021/ja01107A501

    海关参考信息

    专利信息


    专利号:US-7189864-B2
    优先权日:1990-11-19
    标 题:Method of preparing intermediates useful in synthesis of retroviral protease inhibitors
    发明人:NG JOHN S; PRZYBYLA CLAIRE A; MUELLER RICHARD A; VAZQUEZ MICHAEL L; GETMAN DANIEL P
    权利人:SEARLE & CO
    摘要:A synthesis is described for intermediates which are readily amenable to the large scale preparation of hydroxyethylurea-based chiral HIV protease inhibitors. The method includes forming a diastereoselective epoxide from a chiral alpha amino aldehyde.

    专利号:US-5856492-A
    优先权日:1997-01-10
    标题 :Efficient synthesis of a chiral mediator
    发明人:CHEN CHENG YI; XU FENG; TILLYER RICHARD D; ZHAO DALIAN
    权利人:MERCK & CO INC
    摘要:An efficient method for the quantitative preparation and isolation of a compound of formula I ##STR1## or its enantiomer, a chiral mediator used in enantioselective synthesis.

    专利号:US-6022996-A
    优先权日:1990-11-19
    标 题 :Method for making intermediates useful in synthesis of retroviral protease inhibitors
    发明人:NG JOHN S; PRZYBYLA CLAIRE A; MUELLER RICHARD A; VAZQUEZ MICHAEL L; GETMAN DANIEL P
    权利人:SEARLE & CO
    摘要:A synthesis is described for intermediates which are readily amenable to the large scale preparation of hydroxyethylurea-based chiral HIV protease inhibitors. The method includes forming a diastereoselective epoxide from a chiral alpha amino aldehyde.

    专利号:EP-0641333-B1
    优先权日:1992-05-20
    标 题 :Method for making intermediates useful in synthesis of retroviral protease inhibitors
    发明人:NG JOHN S; PRZYBYLA CLAIRE A; MUELLER RICHARD A; VAZQUEZ MICHAEL L; GETMAN DANIEL P
    权利人:SEARLE & CO; MONSANTO CO
    摘要:A synthesis is described for intermediates which are readily amenable to the large scale preparation of hydroxyethylurea-based chiral HIV protease inhibitors. The method includes forming a diastereoselective epoxide compound of formula (I) from a chiral alpha amino aldehyde and halomethyllithium as an organometallic methylene-adding reagent. In formula (I) R<1> is selected from alkyl, aryl, cycloalkyl, cycloalkylalkyl and arylalkyl, which are optionally substituted with a group selected from alkyl, halogen, NO2, OR<9> or SR<9>, where R<9> represents hydrogen or alkyl; and P<1> and P<2> independently are selected from amine protecting groups, including but not limited to, arylalkyl, substituted arylalkyl, cycloalkenylalkyl and substituted cycloalkenylalkyl, allyl, substituted allyl, acyl, alkoxycarbonyl, aralkoxycarbonyl and silyl.

    专利号:EP-0855388-B1
    优先权日:1993-11-23
    标 题 :Method for making intermediates useful in synthesis of retroviral protease inhibitors
    发明人:NG JOHN S; PRZYBYLA CLAIRE A; MUELLER RICHARD A; VAZQUEZ MICHAEL L; GETMAN DANIEL P; FRESKOS JOHN J; DECRESCENZO GARY A; BERTENSHAW DEBORAH E; HEINTZ ROBERT M; ZHANG SUHONG; LIU CHIN; LANEMAN SCOTT A
    权利人:SEARLE & CO
    摘要:A synthesis is described for intermediates which are readily amenable to the large scale preparation of hydroxyethylurea-based chiral HIV protease inhibitors. The method includes forming a cyanohydrin from a chiral alpha amino aldehyde.

    专利号:US-5665827-A
    优先权日:1996-11-07
    标 题:Synthesis of multiblock polymers using group IIA and IIB metal cyclic organometallic initiators
    发明人:HALL JAMES E
    权利人:BRIDGESTONE CORP
    摘要:The invention is a practical process for anionically synthesizing multiblock polymers containing a plurality of blocks formed from polar and/or non-polar monomers by using a cyclic organometallic compound initiator that comprises a divalent metal atom and an organic moiety contained in a ring, preferably a cycloorganomagnesium initiator. Activation of the ring metallic atom results in anionic polymerization of the monomers by addition into the initiator ring at the bonds between the metallic atom and its two adjacent carbon atoms, the metallic atom acting as a bridge between the two living ends of the propagating chain. The active chain ends can be coupled or terminated.

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献

    参考标题:Synthesis Of Binuclear Iridium(III) And Rhodium(III) Complexes Bearing Methylnaphthalene-Linked N-Heterocyclic Carbenes, And Application To Intramolecular Hydroamination
    作者:Kenichi Ogata,Toshinori Nagaya,Shin-Ichi Fukuzawa |发布日期:2010.6
    摘要:With Silver Oxide Followed By [cp∗mcl2]2 (M = Ir, Rh), Binuclear Iridium And Rhodium Complexes 2 Were Formed. Reaction Of These Complexes 2 With Agpf6 Afforded Cl-Bridged Cationic Binuclear Iridium And Rhodium Complexes 3. X-Ray Crystallographic Analysis Of 3 Revealed That The Two Imidazole Rings Of The Carbene Ligand Are In A Parallel Geometry. The Cationic Binuclear Iridium Complexes 3-Ir Could Be

    合成参考文献


    摘要:Schobert, R.; Gordon, G. J., Science of Synthesis, (2004) 27, 1027.
    摘要:Ding, K.; Wang, Z., Science of Synthesis, (2008) 37, 510.
    摘要:Sato, R.; Kimura, T., Science of Synthesis, (2008) 39, 1104.
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