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dendritic alcohol | 219744-41-9

中文名称
——
中文别名
——
英文名称
dendritic alcohol
英文别名
3-[3-(2-benzyloxy-1-(benzyloxymethyl)ethoxy)-2-(2-benzyloxy-1-(benzyloxymethyl)ethoxymethyl)propoxy]-2-[3-(2-benzyloxy-1-(benzyloxymethyl)ethoxy)-2-(2-benzyloxy-1-(benzyloxymethyl)ethoxymethyl)propoxymethyl]propanol;3-[3-[1,3-Bis(phenylmethoxy)propan-2-yloxy]-2-[1,3-bis(phenylmethoxy)propan-2-yloxymethyl]propoxy]-2-[[3-[1,3-bis(phenylmethoxy)propan-2-yloxy]-2-[1,3-bis(phenylmethoxy)propan-2-yloxymethyl]propoxy]methyl]propan-1-ol
dendritic alcohol化学式
CAS
219744-41-9
化学式
C80H98O15
mdl
——
分子量
1299.65
InChiKey
NZQNNFNHFIOYMX-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):
    10.5
  • 重原子数:
    95
  • 可旋转键数:
    53
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    149
  • 氢给体数:
    1
  • 氢受体数:
    15

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:
    dendritic alcoholN-溴代丁二酰亚胺(NBS)三苯基膦 作用下, 以 二氯甲烷 为溶剂, 反应 2.5h, 以98%的产率得到3-(3-[1,3-bis(benzyloxy)-2-propoxy]-2-{[1,3-bis(benzyloxy)-2-propoxy]methyl}propoxy)-2-(3-[1,3-bis(benzyloxy)-2-propoxy]-2-{[1,3-bis(benzyloxy)-2-propoxy]methyl}propoxy)propyl bromide
    参考文献:
    名称:
    使用超滤方法的聚合物支持的寡糖合成。
    摘要:
    使用超滤技术进行聚合物支持的寡糖合成,其中通过具有特定大小孔的膜进行超滤将合成的聚合物结合的寡糖与其他试剂分离。
    DOI:
    10.1039/b705324j
  • 作为产物:
    描述:
    参考文献:
    名称:
    Amphiphilic polyether branched molecules to increase the circulation time of cationic particles
    摘要:
    The preparation, physicochemical and biological properties of amphiphilic polyether branched molecules is described. These 'bunch shaped' molecules when inserted into cationic liposomes/DNA complexes have shown efficient surface charge shielding. As a consequence they efficiently inhibited the non specific interactions with blood components and significantly enhanced circulation time of the particles in the blood track. Formulations containing these molecules compared positively with those containing PEG lipids, providing a 5-fold increase in circulation time. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2007.02.037
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文献信息

  • Synthesis and Surface Functionalization of Aliphatic Polyether Dendrons
    作者:Scott M. Grayson、Jean M. J. Fréchet
    DOI:10.1021/ja001903v
    日期:2000.10.1
    The convergent synthesis and surface modification of a novel family of aliphatic polyether dendrons is described. The synthesis utilizes methallyl dichloride as the monomeric building block along with peripheral benzyl ether and ketal protected hydroxy functionalities. The allylic nature of the electrophilic moieties of methallyl dichloride facilitates their nucleophilic displacement by 2 equiv of
    描述了一种新型脂肪族聚醚树突的聚合合成和表面改性。该合成使用二甲代烯丙基二氯作为单体结构单元以及外围苄醚和缩酮保护的羟基官能团。甲代烯丙基二氯的亲电部分的烯丙基性质促进了它们被 2 当量的适当末端醇基团的亲核置换。在偶联步骤中发挥其活化功能后,烯烃焦点可以通过硼氢化 - 氧化有效地转化为伯醇,导致亲核试剂,然后可以再次偶联到额外的单体上。这些偶联和激活步骤的重复提供了更高代的树突。
  • 1,3-Dipolar cycloaddition reaction of [60]fullerene with thiocarbonyl ylide and synthetic application of the cycloadduct
    作者:Hiroshi Ishida、Kenji Itoh、Masatomi Ohno
    DOI:10.1016/s0040-4020(01)00010-2
    日期:2001.2
    C60 reacted with a thiocarbonyl ylide generated by thermal sila-Pummerer rearrangement of bis(trimethylsilylmethyl) sulfoxide to give a tetrahydrothiophene-fused derivative. The corresponding sulfoxide was obtained by oxidation with m-CPBA and further converted into α-acetoxyltetrahydrothiophene derivative by usual Pummerer rearrangement. The O,S-acetal-like moiety in this compound was utilized for
    C 60与通过双(三甲基甲硅烷基甲基)亚砜的热硅烷-Pummerer重排生成的硫代羰基内酯反应,得到四氢噻吩稠合的衍生物。通过氧化,得到相应的亚砜米-CPBA和进一步转化成通过通常的Pummerer重排α-acetoxyltetrahydrothiophene衍生物。该化合物中的O,S-乙缩醛样部分被用于亲电取代,这对于富勒烯化学是有利的,从而允许在富勒烯表面附近引入各种官能团。
  • Efficient relaxivity enhancement in dendritic gadolinium complexes: effective motional coupling in medium molecular weight conjugates
    作者:David A. Fulton、Mark O'Halloran、David Parker、Kanthi Senanayake、Mauro Botta、Silvio Aime
    DOI:10.1039/b413536a
    日期:——
    Enhancement of the relaxivities of Gd-based MRI contrast agents is achieved by placing the metal ion at the barycentre of the molecular complex in order to improve motional coupling.
    通过将金属离子置于分子复合物的双中心以改善运动耦合,可以增强钆基磁共振成像造影剂的弛豫性。
  • Contrast Agents Endowed with High Relaxivity for Use in Magnetic Resonance Imaging (Mri) Which Contain a Chelating Moiety with Polyhydroxylated Substituents
    申请人:Aime Silvio
    公开号:US20070258905A1
    公开(公告)日:2007-11-08
    The present invention relates to a new class of paramagnetic ion-based contrast agents of molecular weight lower than 3.5 kDa that show a pharmacokinetic profile analogous to that of the commonly used T1-general extravascular agents and that are further characterized by a higher relaxivity.
    本发明涉及一种新的顺磁离子基对比剂,其分子量低于3.5 kDa,显示类似于常用的T1通用非血管内对比剂的药代动力学特征,并且具有更高的弛豫度。
  • Contrast agents endowed with high relaxivity
    申请人:Aime Silvio
    公开号:US20110256067A1
    公开(公告)日:2011-10-20
    The present invention relates to a novel class of paramagnetic ion-based contrast agents of formula (I), wherein a chelating backbone moiety is highly functionalized by the presence of one or more polyhydroxylated chain, that show a pharmacokinetic profile analogous to that of the commonly used T1-general extravascular agents (NSA) but are further characterized by a higher relaxivity.
    本发明涉及一种新型的基于顺磁离子的对比剂类别,其化学式为(I),其中螯合骨架部分通过一个或多个多羟基链的存在高度功能化,表现出与常用的T1通用非血管外用对比剂(NSA)相似的药代动力学特征,但具有更高的弛豫度。
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