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diethyl 2-(4-phenylthiazol-2-yl)phenyl phosphate | 1397690-17-3

中文名称
——
中文别名
——
英文名称
diethyl 2-(4-phenylthiazol-2-yl)phenyl phosphate
英文别名
——
diethyl 2-(4-phenylthiazol-2-yl)phenyl phosphate化学式
CAS
1397690-17-3
化学式
C19H20NO4PS
mdl
——
分子量
389.412
InChiKey
VJVIYMFFNDDLPD-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):
    6.04
  • 重原子数:
    26.0
  • 可旋转键数:
    8.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.21
  • 拓扑面积:
    57.65
  • 氢给体数:
    0.0
  • 氢受体数:
    6.0

反应信息

  • 作为反应物:
    描述:
    diethyl 2-(4-phenylthiazol-2-yl)phenyl phosphate三甲基溴硅烷 、 sodium hydroxide 作用下, 以 二氯甲烷 为溶剂, 反应 8.0h, 以43%的产率得到sodium 2-(4-phenylthiazol-2-yl)phenyl phosphate
    参考文献:
    名称:
    Fluorogenic assay of alkaline phosphatase activity based on the modulation of excited-state intramolecular proton transfer
    摘要:
    A new fluorogenic substrate 1, which enables the fast and quantitative analysis of alkaline phosphatase activity, has been developed. Selective enzymatic hydrolysis of 1 instantly generated fluorescent compound 2 in aqueous media, which undergo an excited-state intramolecular proton transfer process, resulting in a remarkable fluorescence turn-on signal with an unusually large Stokes shift. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.07.021
  • 作为产物:
    描述:
    氯磷酸二乙酯 、 2-(2-hydroxyphenyl)-4-phenylthiazole 在 sodium hydride 作用下, 以 四氢呋喃 、 mineral oil 为溶剂, 反应 48.0h, 以68%的产率得到diethyl 2-(4-phenylthiazol-2-yl)phenyl phosphate
    参考文献:
    名称:
    Fluorogenic assay of alkaline phosphatase activity based on the modulation of excited-state intramolecular proton transfer
    摘要:
    A new fluorogenic substrate 1, which enables the fast and quantitative analysis of alkaline phosphatase activity, has been developed. Selective enzymatic hydrolysis of 1 instantly generated fluorescent compound 2 in aqueous media, which undergo an excited-state intramolecular proton transfer process, resulting in a remarkable fluorescence turn-on signal with an unusually large Stokes shift. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.07.021
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