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sodium (7-methoxy-1,2,2-trimethyl-1,2-dihydroquinolin-4-yl)methanesulfonate | 1345614-47-2

中文名称
——
中文别名
——
英文名称
sodium (7-methoxy-1,2,2-trimethyl-1,2-dihydroquinolin-4-yl)methanesulfonate
英文别名
——
sodium (7-methoxy-1,2,2-trimethyl-1,2-dihydroquinolin-4-yl)methanesulfonate化学式
CAS
1345614-47-2
化学式
C14H18NO4S*Na
mdl
——
分子量
319.357
InChiKey
OHGXMTTUOHAPHG-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):
    -1.14
  • 重原子数:
    21.0
  • 可旋转键数:
    3.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    69.67
  • 氢给体数:
    0.0
  • 氢受体数:
    5.0

反应信息

  • 作为反应物:
    描述:
    sodium (7-methoxy-1,2,2-trimethyl-1,2-dihydroquinolin-4-yl)methanesulfonate五氯化磷三氯氧磷 作用下, 以83%的产率得到(7-methoxy-1,2,2-trimethyl-1,2-dihydroquinolin-4-yl)methanesulfonyl chloride
    参考文献:
    名称:
    Synthesis of Near-IR Fluorescent Oxazine Dyes with Esterase-Labile Sulfonate Esters
    摘要:
    Near-IR oxazine dyes are reported that contain sulfonate esters which are rapidly cleaved by esterase activity to unmask highly polar anionic sulfonates. Strategies for the synthesis of these dyes included the development of milder dye condensation conditions with Improved functional compatibility and the use of an alkyl halide that allows for the Introduction of esterase-labile sulfonates without the need for sulfonation of the target molecule.
    DOI:
    10.1021/ol202619f
  • 作为产物:
    参考文献:
    名称:
    Synthesis of Near-IR Fluorescent Oxazine Dyes with Esterase-Labile Sulfonate Esters
    摘要:
    Near-IR oxazine dyes are reported that contain sulfonate esters which are rapidly cleaved by esterase activity to unmask highly polar anionic sulfonates. Strategies for the synthesis of these dyes included the development of milder dye condensation conditions with Improved functional compatibility and the use of an alkyl halide that allows for the Introduction of esterase-labile sulfonates without the need for sulfonation of the target molecule.
    DOI:
    10.1021/ol202619f
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