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1,11-bis(2-formylphenoxy)-3,6,9-trioxaundecane | 62107-82-8

中文名称
——
中文别名
——
英文名称
1,11-bis(2-formylphenoxy)-3,6,9-trioxaundecane
英文别名
2-[2-[2-[2-[2-(2-formylphenoxy)ethoxy]ethoxy]ethoxy]ethoxy]benzaldehyde
1,11-bis(2-formylphenoxy)-3,6,9-trioxaundecane化学式
CAS
62107-82-8
化学式
C22H26O7
mdl
——
分子量
402.444
InChiKey
RQINLRDIPZLVLB-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    559.2±50.0 °C(Predicted)
  • 密度:
    1.184±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.5
  • 重原子数:
    29
  • 可旋转键数:
    16
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    80.3
  • 氢给体数:
    0
  • 氢受体数:
    7

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    1,11-bis(2-formylphenoxy)-3,6,9-trioxaundecane盐酸羟胺 、 sodium carbonate 作用下, 以 二氯甲烷 为溶剂, 反应 24.0h, 生成
    参考文献:
    名称:
    通过分子内一氧化二氮的二聚合成中型和大型环:高效的CC键形成环封闭反应。
    摘要:
    DOI:
    10.1021/jo991111n
  • 作为产物:
    参考文献:
    名称:
    DIMER COMPOUNDS, AND USE IN BINDING TOXIC REPEATS OF RNA
    摘要:
    本文提供了一些化合物和方法,用于调节基因序列异常重复扩增。更具体地,提供了RNA二聚体抑制剂以及这些抑制剂在调节核苷酸重复扩增方面的用途,例如治疗肌萎缩性脊髓侧索硬化症1型(DM1)、肌萎缩性脊髓侧索硬化症2型(DM2)、Fuchs角膜萎缩症、亨廷顿病、肌萎缩侧索硬化症或额颞型痴呆症。
    公开号:
    US20200207744A1
点击查看最新优质反应信息

文献信息

  • Bentonite Catalyzed an Efficient and Green Synthesis of Arylidene Meldrum's Acid Derivatives in Aqueous Media
    作者:Mahdieh Yahyazadehfar、Sayed Ali Ahmadi、Enayatollah Sheikhhosseini、Dadkhoda Ghazanfari
    DOI:10.2174/1570178617999200807155325
    日期:2021.7
    <p>In the present paper, a simple, highly efficient, and environmentally friendly protocol was proposed for the Knoevenagel condensation reaction of aromatic aldehydes using Meldrum’s acid (2,2-dimethyl-4,6-dioxo-1,3-dioxane) with bentonite as an available non-toxic mineral catalyst exposed to aqueous media under green conditions. Together with the substitution protocol of electron-donating or -withdrawing groups, all reactions were finalized from 5 to 120 min in water at 90°C. With regard to such reactions, the purification of columns on products was not a requirement. Considering the environmental aspect, use of water as a green solvent, utilization of a reusable catalyst, simple work-up process and steps, as well as rapid reaction times were taken into account as some characteristics of these chemical reactions.</p></sec></div> <div class="value-text ch">在本文中,我们提出了一种简单、高效且环保的协议,用于在水相介质下进行芳香醛的Knoevenagel缩合反应。该反应使用Meldrum酸(2,2-二甲基-4,6-二氧杂-1,3-二氧环己烷)作为可用的非有毒矿物催化剂,并与膨润土相结合。在90°C的水中,所有反应在5到120分钟内完成,无需对产物进行柱层析纯化。考虑到环境因素,使用水作为绿色溶剂,利用可重复使用的催化剂,简化了工作过程和步骤,以及快速的反应时间,都是这些化学反应的一些特点。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">One-pot synthesis of nitrones from nitro compounds by in situ trapping of arylhydroxylamines</div> <div class="value"> <div class="value-text"> <span>作者:</span>Foad Kazemi、Moosa Ramdar、Bahram Tavana、Jamal Davarpanah </div> <div class="value-text"> <span>DOI:</span>10.1007/s00706-016-1896-2 </div> <div class="value-text"> <span>日期:</span>2017.6 </div> <div class="value-text en">reduction of the corresponding <span style='color:#ff0000'>nitro</span> <span style='color:#ff0000'>aromatic</span> <span style='color:#ff0000'>compound</span>. Interestingly, the slow and nonselective reduction of nitroarene to arylhydroxylamine step was directed with the condensation of in situ-prepared arylhydroxylamine with <span style='color:#ff0000'>aromatic</span> aldehyde (second step). Moreover, this protocol was successfully used for preparation of valuable dinitrones <span style='color:#ff0000'>from</span> dialdehyde and <span style='color:#ff0000'>nitro</span> <span style='color:#ff0000'>aromatic</span> <span style='color:#ff0000'>compounds</span>. For dinitrone preparation</div> <div class="value-text ch">摘要已经描述了通过使用SnCl 2 ·2H 2 O和Na 2 CO 3将硝基芳烃转化为其相应的硝酮衍生物的高效,方便,简单的方法和高度化学选择性的方法。在无溶剂条件下研磨设备中。可以通过使醛与不稳定的芳基羟胺缩合来获得联芳基硝酮,该芳基羟胺是通过还原相应的硝基芳族化合物就地制备的。有趣的是,将硝基芳烃缓慢且非选择性地还原为芳基羟胺的步骤是通过原位制备的芳基羟胺与芳族醛的缩合进行的(第二步)。此外,该协议已成功用于从二醛和硝基芳族化合物制备有价值的二硝基。为了制备二硝基,首先通过水杨醛和二醇衍生物的反应合成二醛化合物。然后,在我们用于合成联芳基硝酮的最佳条件下,使二醛与还原的硝基化合物反应。 图形概要</div> </div> </li> <li class="feature-list-item"> <div class="content-title">Highly Efficient Ring Closure of Aromatic Dialdehydes to Macrocyclic Allenes</div> <div class="value"> <div class="value-text"> <span>作者:</span>Marcus S. Brody、Robin M. Williams、M. G. Finn </div> <div class="value-text"> <span>DOI:</span>10.1021/ja962868o </div> <div class="value-text"> <span>日期:</span>1997.4.1 </div> <div class="value-text en">The one-pot double deoxygenation of simple alkyl- and polyether-tethered <span style='color:#ff0000'>aromatic</span> dialdehydes to give <span style='color:#ff0000'>macrocyclic</span> allenes has been accomplished in extraordinarily high yield without the need for slow-addition techniques, using a Ti(IV)-substituted ylide reagent and bis(trimethylsilyl)amide bases. Diastereoselective allene formation occurs when a binaphthyl unit is present in the substrate backbone</div> <div class="value-text ch">使用 Ti (IV) 取代的叶立德试剂和双 (三甲基甲硅烷基)酰胺碱。当底物主链中存在联萘单元时,会发生非对映选择性丙二烯形成,所得环状丙二烯通过 X 射线衍射表征。高效环化被认为是关于酰胺碱反离子的预组织和低浓度的 Wittig 型烯化环闭合的直接前体相结合的结果。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">Glaser–Eglinton–Hay sp–sp coupling and macrocyclization: construction of a new class of polyether macrocycles having a 1,3-diyne unit</div> <div class="value"> <div class="value-text"> <span>作者:</span>Naveen Naveen、Srinivasarao Arulananda Babu、Gurpreet Kaur、Nayyar Ahmad Aslam、Maheswararao Karanam </div> <div class="value-text"> <span>DOI:</span>10.1039/c4ra02174f </div> <div class="value-text"> <span>日期:</span>—— </div> <div class="value-text en">skeletally interesting, 18–27 membered, <span style='color:#ff0000'>polyether</span> <span style='color:#ff0000'>macrocycles</span> having a 1,3-diyne unit-based cylindrical backbone are reported. The utility of <span style='color:#ff0000'>polyether</span> <span style='color:#ff0000'>macrocycles</span> having the 1,3-diyne units is shown by incorporating isoxazole and thiophene moieties into the <span style='color:#ff0000'>macrocycles</span>. The structures of representative <span style='color:#ff0000'>crown</span> ether/polyether-type <span style='color:#ff0000'>macrocycles</span> were unambiguously established <span style='color:#ff0000'>from</span> single crystal X-ray structure</div> <div class="value-text ch">据报道,Glaser–Eglinton–Hay型sp–sp偶联,大环化和具有1,3-diyne单元圆柱形主链的骨架结构有趣的18–27元聚醚大环化合物的构建。具有1,3-二炔单元的聚醚大环的用途通过将异恶唑和噻吩部分结合到大环中来显示。从单晶X射线结构分析清楚地建立了代表性的冠醚/聚醚型大环的结构。对代表性大环化合物的X射线结构的研究表明,1,3-二炔单元不是线性的,被发现是弯曲的。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">Aliphatic nitro compounds chemistry: oximes–nitrones tunable production through directed tandem synthesis</div> <div class="value"> <div class="value-text"> <span>作者:</span>Foad Kazemi、Moosa Ramdar、Jamal Davarpanah </div> <div class="value-text"> <span>DOI:</span>10.1007/s00706-018-2326-4 </div> <div class="value-text"> <span>日期:</span>2019.2 </div> <div class="value-text en">AbstractReduction of aliphatic nitro <span style='color:#ff0000'>compounds</span> in the presence of aldehydes and dialdehydes for tunable <span style='color:#ff0000'>directed</span> <span style='color:#ff0000'>synthesis</span> of oximes, nitrones, nitrone–oximes, and dinitrones was reported. The slow and nonselective reduction of aliphatic nitro <span style='color:#ff0000'>compounds</span> was <span style='color:#ff0000'>directed</span> by condensation of in situ prepared alkylhydroxylamines with aromatic aldehydes. Mononitrones and dinitrones were synthesized at reflux</div> <div class="value-text ch">摘要据报导,在醛和二醛存在下还原脂肪族硝基化合物可调谐合成肟,硝酮,硝酮肟和二硝基酮。脂肪族硝基化合物的缓慢且非选择性的还原是通过原位制备的烷基羟胺与芳族醛的缩合来实现的。在四氢呋喃中,使用SnCl 2 ·2H 2 O和Na 2 CO 3分别在回流和55°C条件下合成单硝酮和二硝酮。研究发现,当使用二醛作为醛源时,催化量的羧酸(如3-苯基丙酸)的存在相对于硝酮肟和二肟而言,可以提高二硝酮的收率。 图形概要</div> </div> </li> </ul> <a href="https://chem.molaid.com/material/detail?source=UserSourcePortal&id=3101923r5c72795157N0&inchikey=RQINLRDIPZLVLB-UHFFFAOYSA-N" target="_blank" rel="nofollow" class="view-more">查看更多</a> </div> <div class="module" id="tongleihuahewu"> <h3 class="module-title"><i class="iconfont icon-tongleihuahewu"></i>同类化合物</h3> <div class="compounds-list"> <a target="_blank" href="https://www.molaid.com/MS_152" class="compound-item" title="(2S,3R)-3-(叔丁基)-2-(二叔丁基膦基)-4-甲氧基-2,3-二氢苯并[d][1,3]氧杂磷杂戊环">(2S,3R)-3-(叔丁基)-2-(二叔丁基膦基)-4-甲氧基-2,3-二氢苯并[d][1,3]氧杂磷杂戊环</a> <a target="_blank" href="https://www.molaid.com/MS_155" class="compound-item" 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href="https://www.molaid.com/fenzi/11" class="compound-item" title="苯类化合物">苯类化合物</a> <a href="https://www.molaid.com/fenzi/12" class="compound-item" title="木脂素、新木脂素和相关化合物">木脂素、新木脂素和相关化合物</a> <a href="https://www.molaid.com/fenzi/13" class="compound-item" title="苯丙烷和聚酮">苯丙烷和聚酮</a> <a href="https://www.molaid.com/fenzi/14" class="compound-item" title="脂质和类脂质分子">脂质和类脂质分子</a> <a href="https://www.molaid.com/fenzi/15" class="compound-item" title="有机酸及其衍生物">有机酸及其衍生物</a> <a href="https://www.molaid.com/fenzi/16" class="compound-item" title="有机氧化合物">有机氧化合物</a> <a href="https://www.molaid.com/fenzi/17" class="compound-item" title="生物碱及其衍生物">生物碱及其衍生物</a> <a href="https://www.molaid.com/fenzi/18" class="compound-item" title="有机硫化合物">有机硫化合物</a> <a href="https://www.molaid.com/fenzi/19" class="compound-item" title="核苷、核苷酸和类似物">核苷、核苷酸和类似物</a> <a href="https://www.molaid.com/fenzi/20" class="compound-item" title="碳氢化合物衍生物">碳氢化合物衍生物</a> <a href="https://www.molaid.com/fenzi/21" class="compound-item" title="有机氮化合物">有机氮化合物</a> <a href="https://www.molaid.com/fenzi/22" class="compound-item" title="碳氢化合物">碳氢化合物</a> <a href="https://www.molaid.com/fenzi/23" class="compound-item" title="有机卤素化合物">有机卤素化合物</a> <a href="https://www.molaid.com/fenzi/24" class="compound-item" title="有机聚合物">有机聚合物</a> <a href="https://www.molaid.com/fenzi/25" class="compound-item" title="有机金属化合物">有机金属化合物</a> <a href="https://www.molaid.com/fenzi/26" class="compound-item" title="乙炔化物 ">乙炔化物 </a> <a href="https://www.molaid.com/fenzi/27" class="compound-item" title="有机磷化合物">有机磷化合物</a> <a href="https://www.molaid.com/fenzi/28" class="compound-item" title="叠烯">叠烯</a> <a href="https://www.molaid.com/fenzi/29" class="compound-item" title="有机1,3-偶极化合物">有机1,3-偶极化合物</a> <a href="https://www.molaid.com/fenzi/30" class="compound-item" title="碳化物">碳化物</a> <a href="https://www.molaid.com/fenzi/31" class="compound-item" title="有机盐">有机盐</a> <a href="https://www.molaid.com/fenzi/32" class="compound-item" title="有机阳离子">有机阳离子</a> <a href="https://www.molaid.com/fenzi/33" class="compound-item" title="卡宾">卡宾</a> <a href="https://www.molaid.com/fenzi/34" class="compound-item" title="有机阴离子">有机阴离子</a> </div> </div> </div> <div class="right"> <div class="module"> <link rel="stylesheet" href="https://www.molaid.com/assets/css/common/hot-molecular.css?v=202504271"> <div class="component-card hot-molecular-card" style="--color: #FF4539;"> <div class="title"> <h3 class="title-name">热门分子</h3> </div> <div class="card-content"> <ul class="list"> <li class="item item-special" data-sort="TOP"> <div class="item-img"> <img src="data:image/svg+xml;base64,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