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2-[4-(2,6-diphenyl-pyran-4-ylidenemethyl)-phenylethynyl]-4,6-dimethyl-pyrimidine | 1450722-40-3

中文名称
——
中文别名
——
英文名称
2-[4-(2,6-diphenyl-pyran-4-ylidenemethyl)-phenylethynyl]-4,6-dimethyl-pyrimidine
英文别名
——
2-[4-(2,6-diphenyl-pyran-4-ylidenemethyl)-phenylethynyl]-4,6-dimethyl-pyrimidine化学式
CAS
1450722-40-3
化学式
C32H24N2O
mdl
——
分子量
452.555
InChiKey
CNDFWUVVTIGEIT-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):
    6.99
  • 重原子数:
    35.0
  • 可旋转键数:
    3.0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    35.01
  • 氢给体数:
    0.0
  • 氢受体数:
    3.0

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

  • 作为产物:
    描述:
    2,6-diphenyl-4H-pyran-4-yl triphenylphosphonium tetrafluoroborate salt 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodide正丁基锂potassium carbonate三乙胺 作用下, 以 四氢呋喃甲醇二氯甲烷正戊烷 为溶剂, 反应 0.25h, 生成 2-[4-(2,6-diphenyl-pyran-4-ylidenemethyl)-phenylethynyl]-4,6-dimethyl-pyrimidine
    参考文献:
    名称:
    Methylenepyran based dipolar and quadrupolar dyes: synthesis, electrochemical and photochemical properties
    摘要:
    This paper presents the synthesis of a series of push-pull and quadrupolar pi-conjugated structures incorporating pro-aromatic methylenepyran electron-donor groups and various electron-attracting groups. Some of the methylenepyran derivatives were oxidized by I-2 to give, after reduction by Na2S2O3, bismethylenepyran compounds via successive steps.The electrochemical redox properties of methylenepyrans 5-9 and extended bismethylenepyrans 10, 14, and 15 determined by cyclic voltammetry indicate the formation of redox bistable systems with high bistability. Oxidation of the dimers obtained from 5 to 9 was also described. All compounds are colored and slightly fluorescent (except some bismethylenepyran derivatives). Some compound second-order nonlinear optical properties were investigated, and large positive values of mu beta were obtained. A positive dimer effect was also observed for bispyran derivatives. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2013.07.066
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