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1,5-bis(4-aminobenzoyloxy)pentane | 57609-67-3

中文名称
——
中文别名
——
英文名称
1,5-bis(4-aminobenzoyloxy)pentane
英文别名
Bis(4-aminobenzoic acid)1,5-pentanediyl;5-(4-aminobenzoyl)oxypentyl 4-aminobenzoate
1,5-bis(4-aminobenzoyloxy)pentane化学式
CAS
57609-67-3
化学式
C19H22N2O4
mdl
——
分子量
342.395
InChiKey
KUBBFLRSDLLYKX-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:
    558.0±35.0 °C(Predicted)
  • 密度:
    1?+-.0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.4
  • 重原子数:
    25
  • 可旋转键数:
    10
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    105
  • 氢给体数:
    2
  • 氢受体数:
    6

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

反应信息

  • 作为反应物:
    描述:
    异腈基正丁烷1,5-bis(4-aminobenzoyloxy)pentane邻羧基苯甲醛对甲苯磺酸 作用下, 以 二氯甲烷 为溶剂, 生成 pentane-1,5-diyl bis(4-(1-(butylcarbamoyl)-3-oxoisoindolin-2-yl)benzoate)
    参考文献:
    名称:
    统计数据放大了产品对映体纯度的有机催化双Ugi反应:一种连接物裂解方法,可得到高度对映纯的Ugi产品。
    摘要:
    在这里,我们报告了有机催化双重Ugi反应,在单个操作中将对映选择性过程和ee增强相结合,以提供具有非常高ee值的手性Ugi产品。设计分别由碳酸酯和二酯束缚的双异氰化物和双苯胺,以完成这种双多组分反应,形成10个新的化学键(4个CN,2个CC,2个CO和2个NH键)。该策略进一步用于对映体富集的大环化合物的快速构建。
    DOI:
    10.1021/acs.orglett.9b04239
  • 作为产物:
    描述:
    pentane-1,5-diyl bis-(p-nitrobenzoate) 在 palladium 10% on activated carbon 、 氢气 作用下, 以 乙酸乙酯 为溶剂, 反应 12.0h, 以2705 mg的产率得到1,5-bis(4-aminobenzoyloxy)pentane
    参考文献:
    名称:
    统计数据放大了产品对映体纯度的有机催化双Ugi反应:一种连接物裂解方法,可得到高度对映纯的Ugi产品。
    摘要:
    在这里,我们报告了有机催化双重Ugi反应,在单个操作中将对映选择性过程和ee增强相结合,以提供具有非常高ee值的手性Ugi产品。设计分别由碳酸酯和二酯束缚的双异氰化物和双苯胺,以完成这种双多组分反应,形成10个新的化学键(4个CN,2个CC,2个CO和2个NH键)。该策略进一步用于对映体富集的大环化合物的快速构建。
    DOI:
    10.1021/acs.orglett.9b04239
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文献信息

  • Active-matrix liquid crystal display
    申请人:HITACHI, LTD.
    公开号:EP0806698A1
    公开(公告)日:1997-11-12
    An active-matrix liquid crystal display device employing the in-plane switching mode in which an electric field substantially parallel to the substrate surface is applied to the liquid crystals, characterized by weak torsional anchoring of the liquid crystal molecules (6) and the alignment layer surface at the liquid crystal/alignment layer interface to an extent that the extrapolation length which expresses the strength of said torsional anchoring will become not less than 10% of the gap between the substrates. For obtaining such weak torsional anchoring, an organic alignment layer (5) comprising a polymer and/or oligomer having long-chain alkylene and/or fluoro groups, or an inorganic alignment layer formed by oblique evaporation technique, or a photo-reactive alignment layer formed by linearly polarized light irradiation is used.
    一种采用平面内开关模式的有源矩阵液晶显示装置,在这种模式下,电场基本上平行于基板表面施加到液晶上,其特征是液晶分子(6)和配向层表面在液晶/配向层界面处的扭转锚定很弱,以至于表示所述扭转锚定强度的外推长度将不小于基板之间间隙的 10%。为获得这种微弱的扭转锚定,可使用由具有长链亚烷基和/或氟基团的聚合物和/或低聚物组成的有机配位层 (5),或通过斜蒸发技术形成的无机配位层,或通过线偏振光照射形成的光反应配位层。
  • Composition for interlayer filler of layered semiconductor device, layered semiconductor device, and process for producing layered semiconductor device
    申请人:MITSUBISHI CHEMICAL CORPORATION
    公开号:US10125289B2
    公开(公告)日:2018-11-13
    To provide a composition which satisfies a high K1c value, a high glass transition temperature and a low viscosity simultaneously, and which is capable of forming an interlayer filler layer for a layered semiconductor device of which stable bonding is maintained even regardless of changes of environment. A composition comprising an epoxy compound (A) having a viscosity at 25° C. of at most 50 Pa·s, an amine compound (B) having a melting point or softening point of at least 80° C., and an amine compound (C) having a melting point or softening point of less than 80° C., wherein the proportion of the amine compound (C) is at least 1 part by weight and less than 40 parts by weight per 100 parts by weight of the total amount of the amine compound (B) and the amine compound (C).
    提供一种同时满足高 K1c 值、高玻璃化转变温度和低粘度的组合物,该组合物能够形成层状半导体器件的层间填充层,该层间填充层即使在环境变化的情况下也能保持稳定的结合。 一种组合物,包括在 25 摄氏度时粘度不超过 50 Pa-s 的环氧化合物 (A)、熔点或软化点至少为 80 摄氏度的胺化合物 (B) 以及熔点或软化点低于 80 摄氏度的胺化合物 (C),其中胺化合物 (C) 的比例为每 100 份(重量)胺化合物 (B) 和胺化合物 (C) 的总量中至少 1 份(重量)且少于 40 份(重量)。
  • Synthesis, characterization and morphological studies of some novel siloxane-based block copolymeric materials containing organometallic as well as organic polyesteramides
    作者:Muhammad Saif Ullah Khan、Zareen Akhter、Naseer Iqbal、Mohammad Siddiq
    DOI:10.1016/j.jorganchem.2013.08.002
    日期:2013.11
    A series of semi-aromatic diamine monomers (1,m-bis (4-amino benzoyloxy) alkanes; m = 2-6) having in-built ester linkages with variable methylene spacers were synthesized in two steps from aliphatic diols and p-nitrobenzoyl chloride and characterized by their melting points, elemental analysis, FTIR, H-1 and C-13 NMR spectroscopic studies. The diamines were then polymerized in-situ with ferrocene-based organometallic and terephthaloyl-as well as isophthaloyl-based organic acyl chlorides along with telechelic polydimethylsiloxane oligomer to produce a novel set of ferrocene-containing siloxane-based block copolymers and their organic analogues. The corresponding polyesteramides of the synthesized copolymers, without siloxane segment, were also prepared for comparative studies. The structural features of the organometallic and organic block copolymers along with their respective polyesteramides were confirmed by their physical properties and spectroscopic studies. The molecular parameters of all these materials were determined by static laser light scattering (LLS) technique and glass transition temperatures (T-g) were obtained by differential scanning calorimetry (DSC). The materials were soluble in sulphuric acid and partially soluble in common organic solvents at room temperature, yet become readily soluble upon N-trifluoroacetylation. The morphological information of the synthesized materials was obtained by X-ray diffraction and surface studies (SEM and AFM). (C) 2013 Elsevier B.V. All rights reserved.
  • GREEN, M.
    作者:GREEN, M.
    DOI:——
    日期:——
  • In-plane switching-mode active-matrix liquid crystal display
    申请人:Hitachi, Ltd.
    公开号:EP0806698B1
    公开(公告)日:2005-01-12
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