十九烷-10-胺 | 3241-23-4

• 物质功能分类: 有机原料 - 氨基化合物
• 分子结构分类: 有机化合物 - 有机氮化合物
• 中文名称: 十九烷-10-胺
• 英文名称: 1-nonyldecyl amine
• 英文别名: 10-aminononadecane；nonadecan-10-amine；1-nonyldecylamine；10-nonadecanamine
• CAS: 3241-23-4
• 化学式: C₁₉H₄₁N
• 分子量: 283.541
• InChiKey: DEKCSXCNXGALFT-UHFFFAOYSA-N

物化性质

• 沸点：
  123-124 °C(Press: 0.1 Torr)
• 密度：
  0.8137 g/cm3(Temp: 23 °C)

计算性质

• 辛醇/水分配系数(LogP)：
  8.4
• 重原子数：
  20
• 可旋转键数：
  16
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  26
• 氢给体数：
  1
• 氢受体数：
  1

安全信息

• 海关编码：
  2921199090
• 储存条件：
  存储条件为室温、避光且在惰性气体环境中。

反应信息

• 作为反应物：
  描述：

  十九烷-10-胺 在 甲酸 作用下， 以 二氯甲烷 为溶剂， 反应 9.0h， 生成 4-(2-Carboxyethyl)-4-(1-nonyldecylcarbamoylamino)heptanedioic acid
  参考文献：
  名称：

  Synthesis and antimicrobial activity of symmetrical two-tailed dendritic tricarboxylato amphiphiles

  摘要：

  Two series of water-soluble, symmetrical two-tailed homologous dendritic amphiphiles-R2NCONHC((CH2)(2)COOH)(3), 2(n,n), and R2CHNHCONHC((CH2))(2)COOH)(3), 3(n,n), where R = n-CnH2n+1-were synthesized and compared to R"NHCONHC((CH2)(2)CoOH)(3), 1(n), R" = n-CnH2n+1, to determine whether antimicrobial activity was influenced by total or individual alkyl chain lengths, and whether antimicrobial activity depends on hydrophobicity or tail topology (one or two). In a broad screen of 11 microorganisms, 2(n,n) and 3(n,n) generally displayed higher minimal inhibitory concentrations (MICs) than I(n) against growth as measured by broth microdilution assays. Chain-length specificity was observed against Candida albicans as 1(16), 2(8,8), and 3(8,8) showed the lowest MIC in their respective series. The one case where two-tailed compounds displayed the lowest MICs-3(10,10), 15 mu M; 3(11,11), 7.2 mu M; and 3(12,12), 6.9 mu M-was against Cryptococcus neoformans. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2007.03.017
• 作为产物：
  描述：

  1-溴壬烷 在 palladium on activated charcoal sodium azide 、 氢气 、 碘 、 magnesium 、 三乙胺 作用下， 以 四氢呋喃 、 正己烷 、 N,N-二甲基甲酰胺 为溶剂， 20.0~85.0 ℃ 、427.48 kPa 条件下， 反应 79.25h， 生成 十九烷-10-胺
  参考文献：
  名称：

  Synthesis and antimicrobial activity of symmetrical two-tailed dendritic tricarboxylato amphiphiles

  摘要：

  Two series of water-soluble, symmetrical two-tailed homologous dendritic amphiphiles-R2NCONHC((CH2)(2)COOH)(3), 2(n,n), and R2CHNHCONHC((CH2))(2)COOH)(3), 3(n,n), where R = n-CnH2n+1-were synthesized and compared to R"NHCONHC((CH2)(2)CoOH)(3), 1(n), R" = n-CnH2n+1, to determine whether antimicrobial activity was influenced by total or individual alkyl chain lengths, and whether antimicrobial activity depends on hydrophobicity or tail topology (one or two). In a broad screen of 11 microorganisms, 2(n,n) and 3(n,n) generally displayed higher minimal inhibitory concentrations (MICs) than I(n) against growth as measured by broth microdilution assays. Chain-length specificity was observed against Candida albicans as 1(16), 2(8,8), and 3(8,8) showed the lowest MIC in their respective series. The one case where two-tailed compounds displayed the lowest MICs-3(10,10), 15 mu M; 3(11,11), 7.2 mu M; and 3(12,12), 6.9 mu M-was against Cryptococcus neoformans. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2007.03.017

文献信息

• One-pot multicomponent synthesis of N-sulfonyl amidines using magnetic separable nanoparticles-decorated N-heterocyclic carbene complex with copper
  作者：Arvind Pawar、Shivanand Gajare、Audumbar Patil、Rajanikant Kurane、Gajanan Rashinkar、Suresh Patil

  DOI：10.1007/s11164-021-04455-1

  日期：2021.7

  transmission electron microscopy (TEM) and vibrating sample magnetometer (VSM). MNP[1-Methyl benzimidazole]NHC@Cu complex was successfully implemented as heterogeneous catalyst in one-pot multicomponent synthesis of N-sulfonyl amidines from phenylacetylene, tosyl azide and amines at room temperature. Complex could be recycled six times without significant loss in the yield of product. Graphic abstract

  通过在氯官能化Fe 3 O 4表面共价接枝离子液体如1-甲基苯并咪唑单元，制备了磁性可分离纳米粒子修饰的N-杂环卡宾与铜络合物（MNP[1-甲基苯并咪唑]NHC@Cu）磁性纳米粒子 (MNP)，然后用碘化铜 (I) 进行金属化。MNP[1-甲基苯并咪唑]NHC@Cu复合物已通过不同的技术进行表征，包括傅里叶变换红外（FT-IR）光谱、热重分析（TGA）、能量色散X射线（EDX）分析、X射线衍射（ XRD)、透射电子显微镜 (TEM) 和振动样品磁强计 (VSM)。MNP[1-甲基苯并咪唑]NHC@Cu配合物作为多相催化剂成功应用于室温下苯乙炔、甲苯磺酰叠氮和胺类一锅法多组分合成N-磺酰脒。复合物可以循环使用六次而不会显着降低产品的收率。 图形摘要
• The Synthesis of Perylenebisimide Monocarboxylic Acids
  作者：Heinz Langhals、Wolfgang Lona

  DOI：10.1002/(sici)1099-0690(199805)1998:5<847::aid-ejoc847>3.0.co;2-3

  日期：1998.5

  The synthesis and properties of perylene-bisimides 4 with one carboxylic acid anchor group are described. The properties of 4 are strongly influenced by the spacer between the carboxylic acid group and the imide moeity. Dyes with aliphatic (4d−4g) and aromatic (4a−4c) spacers have been prepared.

  描述了具有一个羧酸锚定基团的苝-双酰亚胺4的合成和性质。4 的性质受到羧酸基团和酰亚胺部分之间的间隔基的强烈影响。已经制备了具有脂肪族 (4d-4g) 和芳香族 (4a-4c) 间隔基的染料。
• Bichromophoric Perylene Derivatives: Energy Transfer from Non-Fluorescent Chromophores
  作者：Heinz Langhals、Sigrid Saulich

  DOI：10.1002/1521-3765(20021216)8:24<5630::aid-chem5630>3.0.co;2-z

  日期：2002.12.16

  The energy of excitation at non-fluorescent chromophores such as fluorenone and anthraquinone has been trapped by a fast energy transfer to the highly fluorescent perylene bisimides. To this end, anthraquinone, fluorenone and anthracene derivatives have been linked to the perylene bisimides by non-conjugating spacers and fluorescence quantum yield of such assemblies have been determined as a function

  在非荧光发色团（例如芴酮和蒽醌）处的激发能量已通过快速转移到高荧光per双酰亚胺中而被捕获。为此，蒽醌，芴酮和蒽衍生物已通过非共轭间隔基与per联双酰亚胺连接，并且已确定了此类组件的荧光量子产率与激发波长的关系。在这种组件中的能量转移受两个生色团的取向的强烈影响。这对于荧光开关的构造是令人感兴趣的。
• Synthesis and Controlled Self-Assembly of Covalently Linked Hexa-<i>peri</i>-hexabenzocoronene/Perylene Diimide Dyads as Models To Study Fundamental Energy and Electron Transfer Processes
  作者：Lukas F. Dössel、Valentin Kamm、Ian A. Howard、Frédéric Laquai、Wojciech Pisula、Xinliang Feng、Chen Li、Masayoshi Takase、Tibor Kudernac、Steven De Feyter、Klaus Müllen

  DOI：10.1021/ja211504a

  日期：2012.4.4

  We report the synthesis and photophysical characterization of a series of hexa-peri-hexabenzocoronene (HBC)/perylenetetracarboxy diimide (PDI) dyads that are covalently linked with a rigid bridge. Both the ratio of the two components and the conjugation of the bridging element are systematically modified to study the influence on self-assembly and energy and electron transfer between electron donor

  我们报告了一系列与刚性桥共价连接的六对六苯并可罗烯 (HBC)/苝四羧基二亚胺 (PDI) 二元组的合成和光物理表征。系统地修改了两种组分的比例和桥接元素的共轭，以研究对电子供体 HBC 和受体 PDI 之间自组装和能量和电子转移的影响。STM 和 2D-​​WAXS 实验表明，无论是在溶液中还是在块状固态中，二元组都组装成有序的二维超分子结构，在纳米尺度上，供体和受体之间的相互方向和距离可控。根据二元组的对称性，观察到具有 HBC 和 PDI 纳米隔离堆叠的柱子或具有交替 HBC 和 PDI 部分的交叉网络。UV-vis、光致发光、瞬态光致发光和瞬态吸收光谱证实，在供体 HBC 光激发后，HBC 和 PDI 之间的光诱导电子转移只能与主要的 Förster 共振能量转移竞争，如果通过 HBC 和 PDI 的紧密堆叠促进有足够的轨道重叠。然而，虽然交替堆叠允许有效的电子转移，但只有纳米隔离
• Analogue synthesis reveals decoupling of antibiofilm and β‐lactam potentiation activities of a lead 2‐aminoimidazole adjuvant against <i>Mycobacterium smegmatis</i>
  作者：Sara E. Martin、Catherine M. Nguyen、Randall J. Basaraba、Christian Melander

  DOI：10.1111/cbdd.13208

  日期：2018.8

  compound evaluating each derivative for biofilm dispersion and β‐lactam potentiation capabilities against M. smegmatis. This study identified a compound that improved upon the biofilm dispersion capabilities of the lead compound. Interestingly, a different compound was identified with an increased ability to potentiate a subset of β‐lactam antibiotics. These compounds indicate that biofilm dispersion

  生物膜形成是细菌在抗生素治疗中幸存下来的许多机制之一。已经证明，当结核分枝杆菌在体外存在于生物膜中时，它表现出对抗菌药物的表型抗性。由于药物治疗后结核分枝杆菌的体内存活可能与生物膜样耐药性表达有关，因此可以推测生物膜分散应增加抗生素敏感性并减少当前抗生素治疗方案的持续时间。以前，我们已经确定了能够分散和抑制结核分枝杆菌和耻垢分枝杆菌的2-氨基咪唑（2-AI）化合物体外生物膜。另外，该化合物增强了羧苄青霉素对结核分枝杆菌的活性，并在较小程度上增强了耻垢分枝杆菌的活性。在这里，我们描述了对该化合物的SAR研究，评估了每种衍生物的生物膜分散性和针对耻垢分枝杆菌的β-内酰胺增强能力。这项研究确定了一种可以改善铅化合物的生物膜分散能力的化合物。有趣的是，鉴定出了一种增强β-内酰胺类抗生素亚型能力的化合物。这些化合物表明生物膜的分散和增强能力可能不相关。

表征谱图