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methanesulfonic acid 2-[4-(7-diethylamino-2-oxo-2H-chromene-3-carbonyl)-2-(2-methanesulfonyloxyethoxy)-phenoxy]-ethyl ester | 338740-60-6

中文名称
——
中文别名
——
英文名称
methanesulfonic acid 2-[4-(7-diethylamino-2-oxo-2H-chromene-3-carbonyl)-2-(2-methanesulfonyloxyethoxy)-phenoxy]-ethyl ester
英文别名
2-[4-[7-(Diethylamino)-2-oxochromene-3-carbonyl]-2-(2-methylsulfonyloxyethoxy)phenoxy]ethyl methanesulfonate
methanesulfonic acid 2-[4-(7-diethylamino-2-oxo-2H-chromene-3-carbonyl)-2-(2-methanesulfonyloxyethoxy)-phenoxy]-ethyl ester化学式
CAS
338740-60-6
化学式
C26H31NO11S2
mdl
——
分子量
597.664
InChiKey
WWUQBMFBAOPFTP-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):
    3.1
  • 重原子数:
    40
  • 可旋转键数:
    15
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    169
  • 氢给体数:
    0
  • 氢受体数:
    12

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
  • 下游产品
    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:
    methanesulfonic acid 2-[4-(7-diethylamino-2-oxo-2H-chromene-3-carbonyl)-2-(2-methanesulfonyloxyethoxy)-phenoxy]-ethyl ester 在 sodium carbonate 、 sodium iodide 作用下, 以 二氯甲烷乙腈 为溶剂, 反应 114.0h, 生成 ({2-[2-[2-(bis-carboxymethyl-amino)-ethoxy]-5-(7-diethylamino-2-oxo-2H-chromene-3-carbonyl)-phenoxy]-ethyl}-carboxymethyl-amino)-acetic acid trifluoroacetic acid salt
    参考文献:
    名称:
    Novel polyaminocarboxylate chelates derived from 3-aroylcoumarins
    摘要:
    We have devised efficient reaction pathways to attach aminopolycarboxylate subunits to the 3-aroylcoumarin chromophore. Two series of compounds were thus prepared in which the chelating arms were directly bonded to the coumarin ring (series A) or to the 3-aroyl moiety (series B). The corresponding Eu(m) and Tb(III) chelates were easily formed and their photophysical properties measured. In all the cases, lanthanide emission lifetimes were in the range of ms. Unfortunately, quantum yields were relatively low. Measurement of T-1 states gave too low range of values to sensitize Tb(m). In fact, the metal emission of Tb(III) chelates of series A was not observed. However, series B was able to sensitize both metals. The absorption/energy-transfer/emission mechanisms are discussed. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(01)00168-5
  • 作为产物:
    描述:
    参考文献:
    名称:
    Novel polyaminocarboxylate chelates derived from 3-aroylcoumarins
    摘要:
    We have devised efficient reaction pathways to attach aminopolycarboxylate subunits to the 3-aroylcoumarin chromophore. Two series of compounds were thus prepared in which the chelating arms were directly bonded to the coumarin ring (series A) or to the 3-aroyl moiety (series B). The corresponding Eu(m) and Tb(III) chelates were easily formed and their photophysical properties measured. In all the cases, lanthanide emission lifetimes were in the range of ms. Unfortunately, quantum yields were relatively low. Measurement of T-1 states gave too low range of values to sensitize Tb(m). In fact, the metal emission of Tb(III) chelates of series A was not observed. However, series B was able to sensitize both metals. The absorption/energy-transfer/emission mechanisms are discussed. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(01)00168-5
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文献信息

  • Novel polyaminocarboxylate chelates derived from 3-aroylcoumarins
    作者:Ernesto Brunet、Marı́a Teresa Alonso、Olga Juanes、Oscar Velasco、Juan Carlos Rodrı́guez-Ubis
    DOI:10.1016/s0040-4020(01)00168-5
    日期:2001.4
    We have devised efficient reaction pathways to attach aminopolycarboxylate subunits to the 3-aroylcoumarin chromophore. Two series of compounds were thus prepared in which the chelating arms were directly bonded to the coumarin ring (series A) or to the 3-aroyl moiety (series B). The corresponding Eu(m) and Tb(III) chelates were easily formed and their photophysical properties measured. In all the cases, lanthanide emission lifetimes were in the range of ms. Unfortunately, quantum yields were relatively low. Measurement of T-1 states gave too low range of values to sensitize Tb(m). In fact, the metal emission of Tb(III) chelates of series A was not observed. However, series B was able to sensitize both metals. The absorption/energy-transfer/emission mechanisms are discussed. (C) 2001 Elsevier Science Ltd. All rights reserved.
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