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[(2S)-1-decoxy-1-oxopropan-2-yl] 4-aminobenzoate | 876665-72-4

中文名称
——
中文别名
——
英文名称
[(2S)-1-decoxy-1-oxopropan-2-yl] 4-aminobenzoate
英文别名
——
[(2S)-1-decoxy-1-oxopropan-2-yl] 4-aminobenzoate化学式
CAS
876665-72-4
化学式
C20H31NO4
mdl
——
分子量
349.47
InChiKey
YTFFIHDVNHQYFC-INIZCTEOSA-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

计算性质

  • 辛醇/水分配系数(LogP):
    6.4
  • 重原子数:
    25
  • 可旋转键数:
    14
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    78.6
  • 氢给体数:
    1
  • 氢受体数:
    5

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:
    [(2S)-1-decoxy-1-oxopropan-2-yl] 4-aminobenzoate三光气乙酸酐三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 3.0h, 生成 4-isocyanobenzoyl-L-lactic acid decyl ester
    参考文献:
    名称:
    Helix-Sense Controlled Polymerization of a Single Phenyl Isocyanide Enantiomer Leading to Diastereomeric Helical Polyisocyanides with Opposite Helix-Sense and Cholesteric Liquid Crystals with Opposite Twist-Sense
    摘要:
    We report the unprecedented helix-sense controlled polymerization of enantiomerically pure phenyl isocyanides bearing an l- or d-alanine pendant with a long alkyl chain. The polymerization with an achiral nickel catalyst diastereoselectively proceeds, resulting in either a right- or left-handed helical polymer, whose helix-sense can be controlled by the polymerization solvent and temperature. Both the diastereomeric right- and left-handed helical polymers further self-assemble into lyotropic cholesteric liquid crystals with opposite twist-senses. Consequently, the macromolecular helicity and mesoscopic, supramolecular cholesteric twist can be controlled by the molecular chirality of the pendant of a single enantiomeric phenyl isocyanide through the polymerization under either kinetic or thermodynamic control assisted by hydrogen bonds. High-resolution atomic force microscopy revealed their helical conformations and enabled the determination of the helical sense.
    DOI:
    10.1021/ja0576536
  • 作为产物:
    描述:
    对硝基苯甲酸4-二甲氨基吡啶 、 palladium on activated charcoal 、 氢气N,N'-二环己基碳二亚胺 作用下, 以 四氢呋喃乙醇二氯甲烷 为溶剂, 反应 33.0h, 生成 [(2S)-1-decoxy-1-oxopropan-2-yl] 4-aminobenzoate
    参考文献:
    名称:
    Helix-Sense Controlled Polymerization of a Single Phenyl Isocyanide Enantiomer Leading to Diastereomeric Helical Polyisocyanides with Opposite Helix-Sense and Cholesteric Liquid Crystals with Opposite Twist-Sense
    摘要:
    We report the unprecedented helix-sense controlled polymerization of enantiomerically pure phenyl isocyanides bearing an l- or d-alanine pendant with a long alkyl chain. The polymerization with an achiral nickel catalyst diastereoselectively proceeds, resulting in either a right- or left-handed helical polymer, whose helix-sense can be controlled by the polymerization solvent and temperature. Both the diastereomeric right- and left-handed helical polymers further self-assemble into lyotropic cholesteric liquid crystals with opposite twist-senses. Consequently, the macromolecular helicity and mesoscopic, supramolecular cholesteric twist can be controlled by the molecular chirality of the pendant of a single enantiomeric phenyl isocyanide through the polymerization under either kinetic or thermodynamic control assisted by hydrogen bonds. High-resolution atomic force microscopy revealed their helical conformations and enabled the determination of the helical sense.
    DOI:
    10.1021/ja0576536
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文献信息

  • Polyisocyanide Derivative Having Controlled Helical Main Chain Structure
    申请人:Okoshi Kento
    公开号:US20090030227A1
    公开(公告)日:2009-01-29
    The object is to provide: a method for producing a polymer having a stable right-handed or left-handed helical structure from a single type of monomer in a per-selective manner and controlling the proportion between a polymer having the right-handed helical structure and a polymer having the left-handed helical structure; and a polymeric material which can be used for the formation of any of the right-handed and left-handed helical structures. Thus, disclosed are: a method for production of a polyisocyanide derivative having a stable helical main chain structure with a right-handed or left-handed helix or a mixture thereof from a single type of monomer by polymerizing an aromatic isocyanate having a substituent harboring a structure —CONH in the aromatic ring and a hydrophobic moiety having 6 or more carbon atoms in a polymerization solvent, wherein the direction of the helix depends on the polarity of the polymerization solvent; a poly(aromatic isocyanide) derivative produced by the method; and an aromatic isocyanide which is useful as a monomer for use in the production of the poly(aromatic isocyanide) derivative.
    本发明旨在提供以下内容:一种从单一类型的单体中以选择性的方式制备具有稳定右旋或左旋螺旋结构的聚合物的方法,并控制具有右旋螺旋结构的聚合物和具有左旋螺旋结构的聚合物之间的比例;以及可用于形成任何右旋和左旋螺旋结构的聚合材料。因此,本发明揭示了:通过在聚合溶剂中聚合具有芳香环上具有结构—CONH的取代基和具有6个或更多碳原子的疏水基团的芳香异氰酸酯,从单一类型的单体中制备具有稳定螺旋主链结构的右旋或左旋螺旋或其混合物的聚异氰酸酯衍生物的制备方法,其中螺旋的方向取决于聚合溶剂的极性;通过该方法制备的聚(芳香异氰酸酯)衍生物;以及用于制备聚(芳香异氰酸酯)衍生物的单体芳香异氰酸酯。
  • US7619109B2
    申请人:——
    公开号:US7619109B2
    公开(公告)日:2009-11-17
  • Helix-Sense Controlled Polymerization of a Single Phenyl Isocyanide Enantiomer Leading to Diastereomeric Helical Polyisocyanides with Opposite Helix-Sense and Cholesteric Liquid Crystals with Opposite Twist-Sense
    作者:Takashi Kajitani、Kento Okoshi、Shin-ichiro Sakurai、Jiro Kumaki、Eiji Yashima
    DOI:10.1021/ja0576536
    日期:2006.1.1
    We report the unprecedented helix-sense controlled polymerization of enantiomerically pure phenyl isocyanides bearing an l- or d-alanine pendant with a long alkyl chain. The polymerization with an achiral nickel catalyst diastereoselectively proceeds, resulting in either a right- or left-handed helical polymer, whose helix-sense can be controlled by the polymerization solvent and temperature. Both the diastereomeric right- and left-handed helical polymers further self-assemble into lyotropic cholesteric liquid crystals with opposite twist-senses. Consequently, the macromolecular helicity and mesoscopic, supramolecular cholesteric twist can be controlled by the molecular chirality of the pendant of a single enantiomeric phenyl isocyanide through the polymerization under either kinetic or thermodynamic control assisted by hydrogen bonds. High-resolution atomic force microscopy revealed their helical conformations and enabled the determination of the helical sense.
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