5,6-dibromoindane | 116631-88-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 茚满类
• 英文名称: 5,6-dibromoindane
• 英文别名: 5,6-dibromo-2,3-dihydro-1H-indene
• CAS: 116631-88-0
• 化学式: C₉H₈Br₂
• 分子量: 275.971
• InChiKey: NWHZTBMZACFTOV-UHFFFAOYSA-N

物化性质

• 熔点：
  76-77 °C
• 沸点：
  142-144 °C(Press: 10 Torr)
• 密度：
  1.828±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.1
• 重原子数：
  11
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

反应信息

• 作为反应物：
  描述：

  5,6-dibromoindane 在 硫酸 、 硝酸 作用下， 生成 5,6-dibromo-4-nitro-indan
  参考文献：
  名称：

  Hogg, Iowa State College Journal of Science, 1945, vol. 20, p. 15,17

  摘要：

  DOI：
• 作为产物：
  描述：

  茚满 在 溴 、 碘 作用下， 以 neat (no solvent) 为溶剂， 以35%的产率得到5,6-dibromoindane
  参考文献：
  名称：

  使用邻二卤代苯衍生苯炔的镍催化电还原合成苯并苯

  摘要：

  描述了通过a)邻-二溴苯或邻-溴芳基磺基氟化物的还原三聚，或b)邻-二溴苯与2,2'-二碘代联苯的还原交叉偶联的电化学镍催化合成三亚苯。前者为在室温下以高达 87% 的分离收率构建苯并苯衍生物提供了一种实用的方法。对于 1,2-二卤代-3-甲基苯和相关的邻位三取代底物，三聚反应以非C 3h对称苯并苯异构体的高底物控制区域选择性进行。

  DOI：

  10.1002/cjoc.202200245

文献信息

• Halogen substituted metallocene compounds for olefin polymerization
  申请人：Voskoboynikov Z. Alexander

  公开号：US20070135595A1

  公开（公告）日：2007-06-14

  A metallocene compound is represented by the formula (1): wherein: M is a Group 3, 4, 5 or 6 transition metal atom, or a lanthanide metal atom, or actinide metal atom, preferably a Group 4 transition metal atom selected from titanium, zirconium or hafnium; E is a substituted or unsubstituted monocyclic or polycyclic arenyl ligand pi-bonded to M; A is a substituted or unsubstituted polycyclic arenyl ligand that is pi-bonded to M and has a different ring structure than the E ligand; at least one of the A and E ligands includes at least one halogen substituent directly bonded to an sp 2 carbon at a bondable ring position; Y is a bridging group containing at least one Group 13, 14, 15, or 16 element and any single position of the ring structure of A and to any single position of the ring structure of E; and y is zero or 1, indicating the absence (y=0) or presence (y=1) of Y; and each X is a univalent anionic ligand, or two X are joined and bound to the metal atom to form a metallocycle ring, or two X are joined to form a chelating ligand, a diene ligand, or an alkylidene ligand; provided that when E is an unsubstituted cyclopentadienyl ligand, either y is one or A is not 2-bromofluorenyl or 2,7-dibromofluorenyl.

  一个茂金属化合物的化学式如下（1）：其中：M是3、4、5或6族过渡金属原子，或镧系金属原子，或锕系金属原子，最好是从钛、锆或铪中选择的4族过渡金属原子；E是与M形成π键的取代或未取代的单环或多环芳基配体；A是与M形成π键且具有不同环结构于E配体的取代或未取代的多环芳基配体；A和E中至少一个包括至少一个卤素取代基，直接连接到可成键环位置的sp2碳上；Y是一个含有至少一个13、14、15或16族元素的桥联基，连接到A和E的环结构的任意单位置；y为0或1，表示Y的存在（y=0）或不存在（y=1）；每个X是一个一价阴离子配体，或两个X连接并与金属原子结合形成一个茂环，或两个X连接形成螯合配体、二烯配体或烷基亚甲基配体；但当E是未取代的环戊二烯基配体时，y为1或A不是2-溴萘基或2,7-二溴萘基。
• Multisubstituted <i>C</i>₂-symmetric <i>ansa</i>-metallocenes bearing nitrogen heterocycles: influence of substituents on catalytic properties in propylene polymerization at higher temperatures
  作者：Pavel S. Kulyabin、Vyatcheslav V. Izmer、Georgy P. Goryunov、Mikhail I. Sharikov、Dmitry S. Kononovich、Dmitry V. Uborsky、Jo Ann M. Canich、Alexander Z. Voskoboynikov

  DOI：10.1039/d1dt00645b

  日期：——

  2′-dibromobiaryls with 4-aminoindenes, which were synthesized via Buchwald–Hartwig reaction or electrophilic amination of 4-indenyl Grignard reagents with trimethylsilylmethyl azide. By a number of examples, the anion-promoted rac-to-meso isomerization method was shown to work reliably well for preparation of rac-ZrMe2-complexes. Certain zirconocenes among the 21 tested in propylene polymerization at

  在这项工作中，我们系统地研究了取代基修饰对基于异特异锆茂催化剂的Me 2 Si（2-Alk-4-（N -carbazolyl）Ind）ZrX 2（X = Cl，Me）性能的影响。 ，其中前体被证明特别适用于高温丙烯聚合工艺。为了获得所需的锆茂，我们开发了一种新的合成途径，即通过Pd催化2，2'-二溴联芳基与4-氨基茚的环化反应，生成4-（N-咔唑基）茚，这是通过Buchwald-Hartwig反应或亲电法合成的用三甲基甲硅烷基甲基叠氮化物将4-茚基格氏试剂胺化。通过许多例子，阴离子促进了外消旋-到-内消旋异构化方法被证明工作良好可靠制备的外消旋-ZrMe 2个-complexes。在MAO或硼酸盐活化下于70和100°C的丙烯聚合中测试的21种茂金属中，某些锆茂在分子量能力，区域选择性或立体选择性方面优于母体催化剂。
• Discovery of (2<i>S</i>)-1-[4-(2-{6-Amino-8-[(6-bromo-1,3-benzodioxol-5-yl)sulfanyl]-9<i>H</i>-purin-9-yl}ethyl)piperidin-1-yl]-2-hydroxypropan-1-one (MPC-3100), a Purine-Based Hsp90 Inhibitor
  作者：Se-Ho Kim、Ashok Bajji、Rajendra Tangallapally、Benjamin Markovitz、Richard Trovato、Mark Shenderovich、Vijay Baichwal、Paul Bartel、Daniel Cimbora、Rena McKinnon、Rosann Robinson、Damon Papac、Daniel Wettstein、Robert Carlson、Kraig M. Yager

  DOI：10.1021/jm3004619

  日期：2012.9.13

  Modulation of Hsp90 (heat shock protein 90) function has been recognized as an attractive approach for cancer treatment, since many cancer cells depend on Hsp90 to maintain cellular homeostasis. This has spurred the search for small-molecule Hsp90 inhibitors. Here we describe our lead optimization studies centered on the purine-based Hsp90 inhibitor 28a containing a piperidine moiety at the purine N9 position. In this study, key SAR was established for the piperidine N-substituent and for the congeners of the 1,3-benzodioxole at C8. These efforts led to the identification of orally bioavailable 28g that exhibits good in vitro profiles and a characteristic molecular biomarker signature of Hsp90 inhibition both in vitro and in vivo. Favorable pharmacokinetic properties along with significant antitumor effects in multiple human cancer xenograft models led to the selection of 28g (MPC-3100) as a clinical candidate.
• 336. Dipole moments and the fixation of aromatic double links: bromohydrindenes and bromotetralins
  作者：Nevil V. Sidgwick、Harold D. Springall

  DOI：10.1039/jr9360001532

  日期：——
• US7446216B2
  申请人：——

  公开号：US7446216B2

  公开（公告）日：2008-11-04