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sodium 9-anthracenesulfonate

中文名称
——
中文别名
——
英文名称
sodium 9-anthracenesulfonate
英文别名
sodium phenanthrene-9-sulfonate;sodium;9-sulfonatophenanthrene
sodium 9-anthracenesulfonate化学式
CAS
——
化学式
C14H9O3S*Na
mdl
——
分子量
280.279
InChiKey
OLMAXHABAMQSLX-UHFFFAOYSA-M
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):
    -0.1
  • 重原子数:
    19
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    65.6
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    碳酸氢钠 作用下, 以 四氯化碳 为溶剂, 反应 0.33h, 生成 sodium 9-anthracenesulfonate
    参考文献:
    名称:
    Niestroj, Michael; Lube, Andreas; Neumann, Wilhelm P., Chemische Berichte, 1995, vol. 128, # 6, p. 575 - 580
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • INK JET TEXTILE PRINTING PENETRANT AND INK JET RECORDING APPARATUS
    申请人:Seiko Epson Corporation
    公开号:EP3124562A2
    公开(公告)日:2017-02-01
    An ink jet textile printing penetrant includes a water-soluble organic solvent; a surfactant; and one type or two or more types selected from the group consisting of a chelating agent and an aromatic compound.
    喷墨纺织品印花渗透剂包括一种溶性有机溶剂;一种表面活性剂;以及一种或两种或两种以上的螯合剂和芳香族化合物。
  • Ink jet textile printing penetrant and ink jet recording apparatus
    申请人:Seiko Epson Corporation
    公开号:US10385223B2
    公开(公告)日:2019-08-20
    An ink jet textile printing penetrant includes a water-soluble organic solvent; a surfactant; and one type or two or more types selected from the group consisting of a chelating agent and an aromatic compound.
    喷墨纺织品印花渗透剂包括一种溶性有机溶剂;一种表面活性剂;以及一种或两种或两种以上的螯合剂和芳香族化合物。
  • Optimization of the synthesis of phenanthrene-2- and -3-sulfonyl chlorides
    作者:V. V. Russkikh、E. A. Khokhrina、V. V. Shelkovnikov
    DOI:10.1134/s1070428012040148
    日期:2012.4
    Sulfonation of phenanthrene with sulfuric acid, followed by neutralization with sodium hydroxide, gave a mixture of isomeric sodium phenanthrenesulfonates in an overall yield of 83%. Sodium phenanthrene-2-, -3-, and -9-sulfonates were isolated in 17, 43, and 4% yield, respectively. Sulfonation of phenanthrene with ClSO3H or SO3 did not improve the yields of phenanthrene-2- and -3-sulfonic acids. Treatment of sodium phenanthrene-2- and -3-sulfonates with PCl5-POCl3 or SOCl2-DMF afforded the corresponding sulfonyl chlorides in 89 and 87 or 69 and 70% yield, respectively. Pure phenanthrene-2- and -3-sulfonyl chlorides were also synthesized in 27 and 51% yield by reaction of a mixture of 2- and 3-sulfonates with PCl5-POCl3.
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