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4,6-bis(octyloxy)benzene-1,3-diamine | 1026350-74-2

中文名称
——
中文别名
——
英文名称
4,6-bis(octyloxy)benzene-1,3-diamine
英文别名
4,6-Dioctoxybenzene-1,3-diamine
4,6-bis(octyloxy)benzene-1,3-diamine化学式
CAS
1026350-74-2
化学式
C22H40N2O2
mdl
——
分子量
364.572
InChiKey
PWIWROGQIOURLL-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:
    506.0±45.0 °C(Predicted)
  • 密度:
    0.977±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    7.3
  • 重原子数:
    26
  • 可旋转键数:
    16
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.73
  • 拓扑面积:
    70.5
  • 氢给体数:
    2
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 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:
    4,6-bis(octyloxy)benzene-1,3-diamine 在 palladium on activated charcoal 氢气三乙胺 作用下, 以 甲醇氯仿 为溶剂, 20.0~48.0 ℃ 、4.0 Pa 条件下, 反应 4.0h, 生成
    参考文献:
    名称:
    月牙芳香寡酰胺的合成
    摘要:
    本文介绍了近年来在我们实验室中开发的新月形(和螺旋形)芳香族寡酰胺的合成方法。提出了衍生自各种四取代苯的各种单体的大规模制备。讨论了构建由间位和间位/对位连接的苯残基组成的各种低聚物的三种不同策略。分析了影响耦合效率和产量的因素。发达的合成方法为更长的低聚物的制备和固相合成的发展提供了基础。
    DOI:
    10.1021/jo050798a
  • 作为产物:
    描述:
    辛醇 在 palladium on activated charcoal 氢气三乙胺 作用下, 20.0 ℃ 、2.67 Pa 条件下, 反应 5.0h, 生成 4,6-bis(octyloxy)benzene-1,3-diamine
    参考文献:
    名称:
    月牙芳香寡酰胺的合成
    摘要:
    本文介绍了近年来在我们实验室中开发的新月形(和螺旋形)芳香族寡酰胺的合成方法。提出了衍生自各种四取代苯的各种单体的大规模制备。讨论了构建由间位和间位/对位连接的苯残基组成的各种低聚物的三种不同策略。分析了影响耦合效率和产量的因素。发达的合成方法为更长的低聚物的制备和固相合成的发展提供了基础。
    DOI:
    10.1021/jo050798a
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文献信息

  • Supramolecular architecture-directed synthesis of a reactive and purely inorganic ladder polyhydrosilsesquioxane
    作者:Zhongjie Ren、Xinyu Cao、Ping Xie、Rongben Zhang、Shouke Yan、Yongmei Ma
    DOI:10.1039/b904057a
    日期:——
    A reactive and purely inorganic high Mw perfect ladder polyhydrosilsesquioxane (H-LPSQ) was first prepared under the direction of two imperative supramolecular architectures: ladder superstructure (H-LS) and donor–acceptor complex (DAC).
    在梯形超结构(H-LS)和供体-受体复合物(DAC)这两种势在必行的超分子结构的指导下,首先制备出了一种活性纯无机高分子量完美梯形聚氢硅烷基二氧杂环戊烷(H-LPSQ)。
  • Hydrogen-Bonding-Mediated Dynamic Covalent Synthesis of Macrocycles and Capsules: New Receptors for Aliphatic Ammonium Ions and the Formation of Pseudo[3]rotaxanes
    作者:Xiao-Na Xu、Lu Wang、Gui-Tao Wang、Jian-Bin Lin、Guang-Yu Li、Xi-Kui Jiang、Zhan-Ting Li
    DOI:10.1002/chem.200900309
    日期:2009.6.2
    Dynamic covalent synthesis! Intramolecular hydrogen‐bonding induces amino‐ and aldehyde‐appended aryl amides to adopt a rigid “V”‐shaped conformation. As a result, stable two‐layered capsules can be assembled quantitatively through the one‐step formation of six imine bonds. The new capsules form complexes with aliphatic diammonium ions to give unique two‐layered pseudo[3]rotaxanes (see figure).
    动态共价合成!分子内氢键诱导基和醛基连接的芳基酰胺采用刚性的“ V”形构象。结果,可以通过一步形成六个亚胺键来定量组装稳定的两层胶囊。新的胶囊与脂肪族二离子形成复合物,从而形成独特的两层假[3]轮烷(见图)。
  • POSITIVE PHOTOSENSITIVE POLYIMIDE RESIN COMPOSITION
    申请人:Nissan Chemical Industries, Ltd.
    公开号:EP1329769A1
    公开(公告)日:2003-07-23
    A novel positive photosensitive resin composition is presented by improving the water repellency at the surface and imparting additional functions to a positive photosensitive resin which can be developed by an alkali aqueous solution and which is excellent in sensitivity and developability, while maintaining such properties. The positive photosensitive polyimide resin composition comprises (a) a solvent-soluble polyimide wherein from 1 to 100 mol% of a bivalent organic group constituting a diamine, has one or more of at least one group selected from the group consisting of a phenolic hydroxyl group, a carboxyl group, a thiophenol group and a sulfonic group, and the reduced viscosity is from 0.05 to 5.0 dl/g (at a concentration of 0.5 g/dl in N-methyl pyrrolidone at a temperature of 30°C), (b) a photosensitive orthoquinonediazide compound, and (c1) a solvent-soluble polyimide wherein from 1 to 100 mol% of a bivalent organic group constituting a diamine, has one or more of at least one group selected from the group consisting of a long chain alkyl group having at least 6 carbon atoms and a fluorinated alkyl group, and the reduced viscosity is from 0.05 to 5.0 dl/g (at a concentration of 0.5g/dl in N-methylpyrrolidone at a temperature of 30°C) or (c2) a polyamic acid wherein from 1 to 100 mol% of a bivalent organic group constituting a diamine, has one or more of at least one group selected from the group consisting of a long chain alkyl having at least 6 carbon atoms and a fluorinated alkyl group, and the reduced viscosity is from 0.05 to 5.0 dl/g (at a concentration of 0.5 g/dl in N-methylpyrrolidone at a temperature of 30°C), wherein component [c1] or component [c2] is from 0.1 to 50 wt%, based on the total weight of all polymers.
    本发明提出了一种新型正性光敏树脂组合物,它通过改善正性光敏树脂表面的憎性和赋予其附加功能,使其可以用碱溶液显影,并在保持这些特性的同时,具有优异的灵敏度和显影性。 正性感光聚酰亚胺树脂组合物包括 (a) 溶剂可溶聚酰亚胺,其中 1 至 100 摩尔%的二价有机基团构成二胺,具有一个或多个至少选自羟基、羧基、噻吩基和磺酸基组成的基团,还原粘度为 0.05 至 5.0 dl/g(在浓度为 0.5克/分升(在N-甲基吡咯烷酮中,温度为30℃),(b)一种光敏原醌噻嗪化合物,和(c1)一种溶剂溶性聚酰亚胺,其中构成二胺的1至100摩尔%的二价有机基团,具有一个或多个至少一个选自至少有6个碳原子的长链烷基和化烷基的基团,且降低的粘度为0.05 至 5.0 分升/克(在 N-甲基吡咯烷酮中的浓度为 0.5 克/分升,温度为 30℃)或 (c2) 聚酰胺酸,其中构成二胺的 1 至 100 摩尔%的二价有机基团具有一个或多个选 自至少具有 6 个碳原子的长链烷基和化烷基组成的组中的至少一个基团,且降粘 度为 0.05至5.0分升/克(在N-甲基吡咯烷酮中浓度为0.5克/分升,温度为30℃时),其中组分[c1]或组分[c2]占所有聚合物总重量的0.1至50重量%。
  • Hydrogen Bonding-Directed Multicomponent Dynamic Covalent Assembly of Mono- and Bimacrocycles. Self-Sorting and Macrocycle Exchange
    作者:Jian-Bin Lin、Xiao-Na Xu、Xi-Kui Jiang、Zhan-Ting Li
    DOI:10.1021/jo801972s
    日期:2008.12.5
    This paper describes the multicomponent dynamic covalent assembly of macrocyclic structures by utilizing hydrogen bonding-driven zigzag anthranilamides as "leading" components. Two or three amino groups have been introduced to one side of hydrogen bonded anthranilamide oligomers. The preorganization of the frameworks enabled the amino groups to condense with structurally matched aldehydes to form mono- and bimacrocycles in good to quantitative yields. Reactions from Lip to five components have been investigated. which involved one-step formation of up to six imine bonds. The preorganization of the templates highly enhanced the stability of the macrocyclic structures. As a result, all the macrocycles Could be purified by simply recrystallizing the Crude products from suitable solvents. Coexisting experiments of three series of three to five components were also performed, which all revealed that the preorganized precursors possessed high self-sorting capacity. On the basis of the same approach, a hydrazone-based macrocycle was also prepared quantitatively, while an intermacrocycle hydrazone-imine exchange was revealed to facilitate the formation of the hydrazone-based macrocycle from an imine-based macrocycle.
  • Feng, Wen; Yamato, Kazuhiro; Yang, Liuqing, Journal of the American Chemical Society, 2009, vol. 131, p. 2629 - 2637
    作者:Feng, Wen、Yamato, Kazuhiro、Yang, Liuqing、Ferguson, Joseph S.、Zhong, Lijian、et al.
    DOI:——
    日期:——
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