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(3,5-di(2-methyl-1-pentoxy)phenyl)-methan-1-ol | 636984-52-6

中文名称
——
中文别名
——
英文名称
(3,5-di(2-methyl-1-pentoxy)phenyl)-methan-1-ol
英文别名
[3,5-Bis(2-methylpentoxy)phenyl]methanol;[3,5-bis(2-methylpentoxy)phenyl]methanol
(3,5-di(2-methyl-1-pentoxy)phenyl)-methan-1-ol化学式
CAS
636984-52-6
化学式
C19H32O3
mdl
——
分子量
308.461
InChiKey
XZBUKPHUYIQNNK-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:
    427.4±30.0 °C(Predicted)
  • 密度:
    0.972±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.4
  • 重原子数:
    22
  • 可旋转键数:
    11
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.68
  • 拓扑面积:
    38.7
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    (3,5-di(2-methyl-1-pentoxy)phenyl)-methan-1-ol 在 lithium aluminium tetrahydride 、 18-冠醚-6偶氮二甲酸二异丙酯potassium carbonate三苯基膦 作用下, 以 四氢呋喃二氯甲烷丙酮 为溶剂, 反应 30.25h, 生成 {3-[3,5-Bis-(2-methyl-pentyloxy)-benzyloxy]-5-[3-(naphthalen-2-yl-phenyl-amino)-benzyloxy]-phenyl}-methanol
    参考文献:
    名称:
    Controlling Solubility and Modulating Peripheral Function in Dendrimer Encapsulated Dyes
    摘要:
    The synthesis of large dendrons and dendrimers with site-isolated dyes at their core has been explored. The dyes selected for this work were coumarin 343 and pentathiophene, as energy transfer processes prevail when the two dyes are intimately mixed but each should behave independently of the other if site-isolation is achieved. Because the two dyes have very different functional characteristics, a protocol involving orthogonal protecting groups and allowing the use of a single family of electroactive dendrons for their encapsulation had to be developed. The synthetic protocol must balance the need to incorporate electroactive groups at the periphery of the dendrons with the requirement for high solubility and a size sufficient to fully encapsulate the central dye. Because of their poor solubility and tendency to crystallize, dendrons with uniform triarylamine substitution proved unsatisfactory leading to the development of new unsymmetrical dendrons with alternating branched alkyl groups and triarylamine moieties at their periphery. These dendrons, which show excellent solubility and no tendency to crystallize, were assembled into large dendrimers using a modular protocol with the light emitting dye at their core. It is expected that the large size of the dendritic shell will provide effective site-isolation for the encapsulated central dyes enabling them to exhibit their intrinsic emission properties with minimal energy transfer between neighboring core fluorophores when processed in bulk thin films.
    DOI:
    10.1021/ja037133f
  • 作为产物:
    描述:
    2-甲基-1-戊醇 在 lithium aluminium tetrahydride 、 三苯基膦偶氮二甲酸二乙酯 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 反应 14.25h, 生成 (3,5-di(2-methyl-1-pentoxy)phenyl)-methan-1-ol
    参考文献:
    名称:
    Controlling Solubility and Modulating Peripheral Function in Dendrimer Encapsulated Dyes
    摘要:
    The synthesis of large dendrons and dendrimers with site-isolated dyes at their core has been explored. The dyes selected for this work were coumarin 343 and pentathiophene, as energy transfer processes prevail when the two dyes are intimately mixed but each should behave independently of the other if site-isolation is achieved. Because the two dyes have very different functional characteristics, a protocol involving orthogonal protecting groups and allowing the use of a single family of electroactive dendrons for their encapsulation had to be developed. The synthetic protocol must balance the need to incorporate electroactive groups at the periphery of the dendrons with the requirement for high solubility and a size sufficient to fully encapsulate the central dye. Because of their poor solubility and tendency to crystallize, dendrons with uniform triarylamine substitution proved unsatisfactory leading to the development of new unsymmetrical dendrons with alternating branched alkyl groups and triarylamine moieties at their periphery. These dendrons, which show excellent solubility and no tendency to crystallize, were assembled into large dendrimers using a modular protocol with the light emitting dye at their core. It is expected that the large size of the dendritic shell will provide effective site-isolation for the encapsulated central dyes enabling them to exhibit their intrinsic emission properties with minimal energy transfer between neighboring core fluorophores when processed in bulk thin films.
    DOI:
    10.1021/ja037133f
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文献信息

  • Controlling Solubility and Modulating Peripheral Function in Dendrimer Encapsulated Dyes
    作者:Paul Furuta、Jean M. J. Fréchet
    DOI:10.1021/ja037133f
    日期:2003.10.1
    The synthesis of large dendrons and dendrimers with site-isolated dyes at their core has been explored. The dyes selected for this work were coumarin 343 and pentathiophene, as energy transfer processes prevail when the two dyes are intimately mixed but each should behave independently of the other if site-isolation is achieved. Because the two dyes have very different functional characteristics, a protocol involving orthogonal protecting groups and allowing the use of a single family of electroactive dendrons for their encapsulation had to be developed. The synthetic protocol must balance the need to incorporate electroactive groups at the periphery of the dendrons with the requirement for high solubility and a size sufficient to fully encapsulate the central dye. Because of their poor solubility and tendency to crystallize, dendrons with uniform triarylamine substitution proved unsatisfactory leading to the development of new unsymmetrical dendrons with alternating branched alkyl groups and triarylamine moieties at their periphery. These dendrons, which show excellent solubility and no tendency to crystallize, were assembled into large dendrimers using a modular protocol with the light emitting dye at their core. It is expected that the large size of the dendritic shell will provide effective site-isolation for the encapsulated central dyes enabling them to exhibit their intrinsic emission properties with minimal energy transfer between neighboring core fluorophores when processed in bulk thin films.
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