5-丁基-壬烷 | 17312-63-9

• 分子结构分类: 有机化合物 - 碳氢化合物 - 饱和烃
• 中文名称: 5-丁基-壬烷
• 英文名称: 5-butylnonane
• 英文别名: 5-butyl-nonane；5-Butyl-nonan；5-Butylnonan；tributylmethane
• CAS: 17312-63-9
• 化学式: C₁₃H₂₈
• mdl: MFCD09038365
• 分子量: 184.365
• InChiKey: YXSQPZMAIVSYDV-UHFFFAOYSA-N

物化性质

• 熔点：
  -28.13°C (estimate)
• 沸点：
  217.5°C
• 密度：
  0.7635
• 保留指数：
  1204

计算性质

• 辛醇/水分配系数(LogP)：
  7
• 重原子数：
  13
• 可旋转键数：
  9
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

安全信息

• 海关编码：
  2901100000

反应信息

• 作为反应物：
  描述：

  5-丁基-壬烷 在 aluminum oxide 、 氯化亚砜 、 copper(II) oxide 、 zinc(II) oxide 、 sodium hydroxide 、 zinc(II) chloride 作用下， 以 氯仿 、 水 为溶剂， 反应 8.0h， 生成
  参考文献：
  名称：

  含有液晶基元的内酯芳族衍生物及制备方法 和侧链型液晶聚合物及其制备方法与应用

  摘要：

  本发明公开了一种含有液晶基元的内酯芳族衍生物及制备方法，以及由该含有液晶基元的内酯芳族衍生物作为聚合单体制备的侧链型液晶聚合物及其制备方法与应用。本发明首先采用有机合成方法制备含液晶基元的内酯衍生物，再利用开环聚合方法制备侧链型液晶聚合物，反应步骤简单，反应条件温和，且可通过控制引发剂及聚合单体的投料比合成指定分子量的聚合物。制备的侧链型液晶聚合物符合注塑、模压、挤出、涂覆等常规方法的加工要求。能够用于显示、光学记录、色谱分离、相变储能、生物组织恢复等领域。

  公开号：

  CN110483458B
• 作为产物：
  描述：

  5-壬酮 在 乙醚 、 草酸 、 溶剂黄146 、 铂 作用下， 生成 5-丁基-壬烷
  参考文献：
  名称：

  Iwanow, Bulletin de la Societe Chimique de France, 1925, vol. <4>37, p. 289,293

  摘要：

  DOI：

文献信息

• Cross coupling reactions of multiple CCl bonds of polychlorinated solvents with Grignard reagent using a pincer nickel complex
  作者：Yashraj Gartia、Abhijit Biswas、Matthew Stadler、Udaya Bhasker Nasini、Anindya Ghosh

  DOI：10.1016/j.molcata.2012.07.007

  日期：2012.11

  The nickel(II) complex of a bulky pincer-type ligand, N,N′-bis(2,6-diisopropylphenyl)-2,6-pyridinedicarboxamido, was examined for sp3–sp3 coupling of Grignard reagents with polychlorinated solvents. The nickel(II) complex catalyzed CC coupling of polychlorinated alkyl halides, such as dichloromethane (CH2Cl2), chloroform (CHCl3), and carbon tetrachloride (CCl4), with various Grignard reagents. The

  检查了大钳形配体N，N'-双（2,6-二异丙基苯基）-2,6-吡啶二甲酰胺基的镍（II）配合物与多氯溶剂的格氏试剂的sp 3 –sp 3偶联。镍（II）络合物通过各种格氏试剂催化多氯代烷基卤化物（例如二氯甲烷（CH 2 Cl 2），氯仿（CHCl 3）和四氯化碳（CCl 4））的CC偶联。在环境反应条件下并在短时间内（20分钟）内进行了多个CCl键的有效活化。该催化剂显示出该反应类型迄今报道的最高活性，催化剂负载量低至0.4 mol％，周转频率（TOF）高达724 h-1。对于正在研究的所有多氯代溶剂，该催化剂均能够通过CC键形成取代所有氯原子。催化过程可能被证明是补救有毒多氯溶剂的有效方法，同时可产生合成和商业上重要的化学物质。
• A Novel Iron Complex for Cross-Coupling Reactions of Multiple C–Cl Bonds in Polychlorinated Solvents with Grignard Reagents
  作者：Yashraj Gartia、Sharon Pulla、Punnamchandar Ramidi、Carolina Costa Farris、Zeid Nima、Darin E. Jones、Alexandru S. Biris、Anindya Ghosh

  DOI：10.1007/s10562-012-0913-2

  日期：2012.11

  A novel iron(III) complex (2) of a pincer ligand [1, N2,N6-bis(2,6-diisopropylphenyl)pyridine-2,6-dicarboxamide] was developed and used for remediation of polychlorinated solvents via sp(3)-sp(3) coupling of Grignard reagents with C-Cl bonds. The use of an iron catalyst for such coupling reactions is highly desirable due to its greener and more economical nature. Complex 2 was characterized using various spectroscopic techniques: electrospray ionization mass spectrometer (ESI-MS, m/z 575.1), cyclic voltammetry (E-1/2, 0.03 V and Delta E, 0.97 V), and ultraviolet visible (UV/Vis) spectroscopic techniques. The iron(III) complex showed efficient activation of multiple C-Cl bonds and catalyzing C-C coupling of polychlorinated alkyl halides, such as dichloromethane (CH2Cl2), chloroform (CHCl3), and carbon tetrachloride (CCl4), with various Grignard reagents under ambient reaction conditions. Complex 2 showed exceptional activity with reactions approaching near completion in about 5 min. With the required catalyst loading as low as 0.2 mol%, considerably high turnover numbers (TON = 483) and turnover frequency (TOF = 5,800 h(-1)) were obtained. None of the products detected during the reaction contained any chlorine, indicating an efficient dechlorination method while synthesizing products of synthetic and commercial interest. Interestingly, the catalyst was capable of replacing all chlorine atoms in each polychlorinated solvent under the investigations with high conversion.
• Karrer; Ferri, Helvetica Chimica Acta, 1934, vol. 17, p. 361
  作者：Karrer、Ferri

  DOI：——

  日期：——
• Mineralogy of Tagish Lake: An ungrouped type 2 carbonaceous chondrite
  作者：M. E. Zolensky、K. Nakamura、M. Gounelle、T. Mikouchi、T. Kasama、O. Tachikawa、E. Tonui

  DOI：10.1111/j.1945-5100.2002.tb00852.x

  日期：2002.5

  Abstract— In this paper we describe the recovery, handling and preliminary mineralogical investigation of the Tagish Lake meteorite. Tagish Lake is a type 2 carbonaceous chondrite which bears similarities to CI1 and CM chondrite groups, but is distinct from both. Abundant phyllosilicates as well as chondrules (however sparse) and common olivine grains in the matrix preclude any other classification. The bulk density of Tagish Lake (1.67 g/cc) is far lower than CI or CM chondrites (2.2‐2.3 and 2.6‐2.9 g/cc, respectively), or any other meteorite for that matter. We have identified two lithologies: a dominant carbonate‐poor lithology and a less‐abundant carbonate‐rich lithology. The meteorite is a breccia at all scales.We have noted similarities between Tagish Lake and some clasts within the enigmatic meteorite Kaidun; possibly there are genetic relationships here worth exploring. In the paper we describe a clast of CM1 material within Tagish Lake which is very similar to a major lithology in Kaidun.
• Petrow; Tschernyschew, Doklady Akademii Nauk SSSR, 1949, vol. 67, p. 1047
  作者：Petrow、Tschernyschew

  DOI：——

  日期：——

表征谱图