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Acetic acid 3''-benzyloxy-3',2''-dihydroxy-2,2'-dimethoxy-[1,1';4',1'']ternaphthalen-3-yl ester | 300533-66-8

中文名称
——
中文别名
——
英文名称
Acetic acid 3''-benzyloxy-3',2''-dihydroxy-2,2'-dimethoxy-[1,1';4',1'']ternaphthalen-3-yl ester
英文别名
[4-[3-hydroxy-4-(2-hydroxy-3-phenylmethoxynaphthalen-1-yl)-2-methoxynaphthalen-1-yl]-3-methoxynaphthalen-2-yl] acetate
Acetic acid 3''-benzyloxy-3',2''-dihydroxy-2,2'-dimethoxy-[1,1';4',1'']ternaphthalen-3-yl ester化学式
CAS
300533-66-8
化学式
C41H32O7
mdl
——
分子量
636.701
InChiKey
KLMDRJSRNVTURJ-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):
    9.4
  • 重原子数:
    48
  • 可旋转键数:
    9
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    94.4
  • 氢给体数:
    2
  • 氢受体数:
    7

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

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文献信息

  • Recognition of the chain length of α,ω-diamines by a meso-ternaphthalene derivative with two crown ethers
    作者:Kazunori Tsubaki、Hiroyuki Tanaka、Takumi Furuta、Takayoshi Kinoshita、Kaoru Fuji
    DOI:10.1016/s0040-4039(00)01018-2
    日期:2000.8
    A new ditopic receptor 2 consisting of a meso-ternaphthalene backbone and two crown rings has been shown to selectively complex and transfer dipicrate of 1,9-diaminononane and 1,10-diaminodecane from aqueous solution into the organic phase.
    已经显示了一种新的二位受体2,它由内-间骨架和两个冠环组成,可以选择性地将1,9-二壬烷和1,10-二癸烷的二尖晶石络合物从溶液中转移到有机相中。
  • Use of meso-ternaphthalene derivatives: linear recognition of the α,ω-diamines by homoditopic receptors
    作者:Kazunori Tsubaki、Hiroyuki Tanaka、Takumi Furuta、Kiyoshi Tanaka、Takayoshi Kinoshita、Kaoru Fuji
    DOI:10.1016/s0040-4020(02)00547-1
    日期:2002.7
    The new ditopic receptors 1-3 consisting of a meso-ternaphthalene backbone and two crown ether rings have been synthesized. Hosts 2 and 3 have been shown to selectively complex and transfer the dipicrates, 1,9-diaminononane and 1,10-diaminodecane, from aqueous solution into the organic phase. (C) 2002 Elsevier Science Ltd. All rights reserved.
  • Configurationally defined sexi- and octinaphthalene derivatives: synthesis and optical properties
    作者:Takumi Furuta、Kiyoshi Tanaka、Kazunori Tsubaki、Kaoru Fuji
    DOI:10.1016/j.tet.2004.03.055
    日期:2004.5
    The copper mediated oxidative coupling of optically active quaternaphthalenes having a 2-hydroxynaphthyl moiety gave configurationally defined optically active octinaphthalenes. The absolute configuration was determined by comparison with products of [6+2] coupling. The CD spectra of bi-, ter-, quater-, sexi- and octinaphthalenes suggested that the absolute configuration of the chiral axis could be deduced from the intensity of their Cotton effects. (C) 2004 Published by Elsevier Ltd.
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