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2,5-diiodo-4-octyloxyphenol | 911307-60-3

中文名称
——
中文别名
——
英文名称
2,5-diiodo-4-octyloxyphenol
英文别名
2,5-Diiodo-4-octoxyphenol;2,5-diiodo-4-octoxyphenol
2,5-diiodo-4-octyloxyphenol化学式
CAS
911307-60-3
化学式
C14H20I2O2
mdl
——
分子量
474.121
InChiKey
UZMDRMOEWKXPNC-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

计算性质

  • 辛醇/水分配系数(LogP):
    6.3
  • 重原子数:
    18
  • 可旋转键数:
    8
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    29.5
  • 氢给体数:
    1
  • 氢受体数:
    2

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:
    2,5-diiodo-4-octyloxyphenol 在 palladium diacetate 三乙胺三苯基膦三(邻甲基苯基)磷偶氮二甲酸二乙酯 作用下, 以 四氢呋喃N,N-二甲基甲酰胺 为溶剂, 反应 48.0h, 生成 Methyl-[4-(4-nitro-phenylazo)-phenyl]-{2-[4-octyloxy-2,5-bis-((E)-styryl)-phenoxy]-ethyl}-amine
    参考文献:
    名称:
    Synthesis of double-conjugated-segment molecules and their application as ultra-broad two-photon-absorption optical limiters
    摘要:
    合成了一系列新型双共轭段分子,其中两个共轭段由醚链分隔,这些化合物提供了非常宽的双光子吸收光谱范围,满足了光学限幅领域内的迫切需求。
    DOI:
    10.1039/b208190c
  • 作为产物:
    描述:
    1,4-二碘-2,5-二(辛基氧基)苯三溴化硼 作用下, 以 二氯甲烷 为溶剂, 反应 4.0h, 以81%的产率得到2,5-diiodo-4-octyloxyphenol
    参考文献:
    名称:
    Controlled dealkylation by BBr3: efficient synthesis of para-alkoxy-phenols
    摘要:
    Controlled dealkylation of dialkyl-aryl-ethers by substoichiometric BBr3 has been developed as a general tool for the differentiation of the oxygen functions in hydroquinone derivatives. The reaction proceeds smoothly at rt either on linear or branched alkyl-ethers and provides the corresponding p-alkoxy-phenols RO-Ar-OH in high yields. With respect to the conventional alkylation path of Ar(OH)(2), this process represents a tunable and convenient route to key intermediates for conjugated materials with differentiated side chains. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2012.08.132
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文献信息

  • Amphiphilic polymers functionalized with glucose or a derivative thereof
    申请人:Synchimia S.r.l.
    公开号:EP2620461A1
    公开(公告)日:2013-07-31
    Amphiphilic polymers functionalized with glucose or derivatives thereof are described, in particular poly(p-phenylene ethynylene) substituted by a molecule of glucose or a derivative thereof. Said polymers find advantageous use in the field of fluorescence-quenching optical sensors or in the field of OLEDs (Organic Light Emitting Diodes).
    本文介绍了用葡萄糖或其衍生物官能化的两性聚合物,特别是由葡萄糖分子或其衍生物取代的聚对苯乙炔。这些聚合物在荧光淬灭光学传感器或有机发光二极管(OLED)领域具有优势。
  • Synthesis of double-conjugated-segment molecules and their application as ultra-broad two-photon-absorption optical limiters
    作者:Junxiang Zhang、Yiping Cui、Mingliang Wang、Juzheng Liu
    DOI:10.1039/b208190c
    日期:2002.10.18
    A series of novel double-conjugated-segment molecules, in which two conjugated segments are separated by an ether chain, were synthesized; these compounds provide a very broad two-photon absorption spectral range, which satisfies an urgent need in the optical limiting area.
    合成了一系列新型双共轭段分子,其中两个共轭段由醚链分隔,这些化合物提供了非常宽的双光子吸收光谱范围,满足了光学限幅领域内的迫切需求。
  • Controlled dealkylation by BBr3: efficient synthesis of para-alkoxy-phenols
    作者:Chiara Pasquini、Alessandra Coniglio、Mauro Bassetti
    DOI:10.1016/j.tetlet.2012.08.132
    日期:2012.11
    Controlled dealkylation of dialkyl-aryl-ethers by substoichiometric BBr3 has been developed as a general tool for the differentiation of the oxygen functions in hydroquinone derivatives. The reaction proceeds smoothly at rt either on linear or branched alkyl-ethers and provides the corresponding p-alkoxy-phenols RO-Ar-OH in high yields. With respect to the conventional alkylation path of Ar(OH)(2), this process represents a tunable and convenient route to key intermediates for conjugated materials with differentiated side chains. (C) 2012 Elsevier Ltd. All rights reserved.
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