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3,4,5-tris(tetraethyleneoxy)benzoyl chloride | 887501-25-9

中文名称
——
中文别名
——
英文名称
3,4,5-tris(tetraethyleneoxy)benzoyl chloride
英文别名
Cl(O)C-Ph((EO)4OMe)3;3,4,5-Tris[(2,5,8,11-tetraoxatridecan-13-yl)oxy]benzoyl chloride;3,4,5-tris[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethoxy]benzoyl chloride
3,4,5-tris(tetraethyleneoxy)benzoyl chloride化学式
CAS
887501-25-9
化学式
C34H59ClO16
mdl
——
分子量
759.286
InChiKey
JGNVRJQGMZCGQH-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):
    0.6
  • 重原子数:
    51
  • 可旋转键数:
    40
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.79
  • 拓扑面积:
    156
  • 氢给体数:
    0
  • 氢受体数:
    16

反应信息

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文献信息

  • Non-coordinating anions assemble cyanine amphiphiles into ultra-small fluorescent nanoparticles
    作者:Ievgen Shulov、Youri Arntz、Yves Mély、Vasyl G. Pivovarenko、Andrey S. Klymchenko
    DOI:10.1039/c6cc03716j
    日期:——

    A non-coordinating anion, fluorinated tetraphenylborate, assembles specially designed cationic cyanine amphiphiles into 7–8 nm fluorescent nanoparticles that are >40-fold brighter than a single cyanine dye.

    一种不协同的阴离子,化四苯基硼酸盐,将特别设计的阳离子青霉烷两亲分子组装成直径为7-8纳米的荧光纳米颗粒,其亮度比单个青霉烷染料高出40倍以上。
  • MODIFIED POLY(PROPYLENE-IMINE) DENDRIMERS AND THEIR USE AS TRANSFECTION AGENTS FOR AMIONIC BIOACTIVE FACTORS ( as amended
    申请人:Tack Frederik
    公开号:US20100298403A1
    公开(公告)日:2010-11-25
    The present invention is concerned with modified poly-(propylene imine) dendrimers, comprising cationic internal ammonium groups and external non-toxic endgroups, pharmaceutical compositions comprising said dendrimers, methods for the production of said dendrimers and their use as transfections agents for anionic bioactive therapeutic factors, for use in gene therapy, in particular for the treatment of cancer. The modified poly-(propylene imine) dendrimer of generation 1, 2, 3, 4 or 5, also comprising incomplete dendrimers and mixtures thereof, comprising external end groups and internal amine functions are characterized in that: (a) substantially all external endgroups are groups of formula (I) wherein R is a radical selected from the group of C 1-10 alkyl, polyethylene glycol radical and polyethylene glycol gallyl radical; and (b) substantially all internal amine functions are quaternary cationic ammonium functions. Most preferred are the quaternized compounds DAB-dendr-(NHCOCH 3 ) 4 , DAB-dendr-(NHCOCH 3 ) 8 , DAB-dendr-(NHCOCH 3 ) 16 , DAB-dendr-(NHCOCH 3 ) 32 , DAB-dendr-(NHCOCH 3 ) 64 , DAB-dendr-(NHCOPh((EO) 4 OMe) 3 ) 4 , DAB-dendr-(NHCOPh((EO) 4 OMe) 3 ) 8 , DAB-dendr-(NHCOPh((EO) 4 OMe) 3 ) 16 , DAB-dendr-(NHCOPh((EO) 4 OMe) 3 ) 32 and DAB-dendr-(NHCOPh((EO) 4 OMe) 3 ) 64 .
  • [EN] DENDRITIC MOLECULES, PROCESS FOR THEIR PREPARATION AND USES THEREOF<br/>[FR] MOLÉCULES DENDRITIQUES, LEUR PROCÉDÉ DE PRÉPARATION ET LEURS UTILISATIONS
    申请人:[en]SUPERBRANCHE
    公开号:WO2023198813A1
    公开(公告)日:2023-10-19
    The present invention relates to polyfunctional organic dendritic molecules derived from alkyl phosphonates or esters, to a process for preparing the same and to the use thereof, in particular as drug carriers or contrast agents.
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