摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

N-(4-(1,2,3,4,5,6,7,8,9,10-decahydro-3,3,6,6-tetramethyl-1,8-dioxoacridin-9yl)phenyl)acetamide | 392722-30-4

中文名称
——
中文别名
——
英文名称
N-(4-(1,2,3,4,5,6,7,8,9,10-decahydro-3,3,6,6-tetramethyl-1,8-dioxoacridin-9yl)phenyl)acetamide
英文别名
N-[4-(3,3,6,6-tetramethyl-1,8-dioxo-2,4,5,7,9,10-hexahydroacridin-9-yl)phenyl]acetamide
N-(4-(1,2,3,4,5,6,7,8,9,10-decahydro-3,3,6,6-tetramethyl-1,8-dioxoacridin-9yl)phenyl)acetamide化学式
CAS
392722-30-4
化学式
C25H30N2O3
mdl
——
分子量
406.525
InChiKey
UEGBANYAKOJYOS-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):
    3.2
  • 重原子数:
    30
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    75.3
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    对乙酰氨基苯甲醛5,5-二甲基-1,3-环己二酮 在 ammonium acetate 作用下, 反应 0.25h, 以75%的产率得到N-(4-(1,2,3,4,5,6,7,8,9,10-decahydro-3,3,6,6-tetramethyl-1,8-dioxoacridin-9yl)phenyl)acetamide
    参考文献:
    名称:
    MCM-41-SO3H as a nanoreactor for the one-pot, solvent-free synthesis of 1,8-dioxo-9-aryl decahydroacridines
    摘要:
    AbstractOne‐pot four‐component synthesis of 1,8‐dioxo‐9‐aryl decahydroacridines in solvent‐free condition was efficiently performed in the presence of MCM‐41‐SO3H as a nanocatalyst and nanoreactor in good yields. The method provides several advantages such as low cost, operational and experimental simplicity, high yields, and short reaction times. J. Heterocyclic Chem., (2012).
    DOI:
    10.1002/jhet.692
点击查看最新优质反应信息

文献信息

  • MCM-41-SO3H as a nanoreactor for the one-pot, solvent-free synthesis of 1,8-dioxo-9-aryl decahydroacridines
    作者:Shahnaz Rostamizadeh、Asiyeh Amirahmadi、Nasrin Shadjou、Ali M. Amani
    DOI:10.1002/jhet.692
    日期:2012.1
    AbstractOne‐pot four‐component synthesis of 1,8‐dioxo‐9‐aryl decahydroacridines in solvent‐free condition was efficiently performed in the presence of MCM‐41‐SO3H as a nanocatalyst and nanoreactor in good yields. The method provides several advantages such as low cost, operational and experimental simplicity, high yields, and short reaction times. J. Heterocyclic Chem., (2012).
查看更多