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10-hydroxy-9-(4-methoxyphenyl)-3,3,6,6-tetramethyl-1,2,3,4,5,6,7,8,9,10-decahydroacridine-1,8-dione | 676349-08-9

中文名称
——
中文别名
——
英文名称
10-hydroxy-9-(4-methoxyphenyl)-3,3,6,6-tetramethyl-1,2,3,4,5,6,7,8,9,10-decahydroacridine-1,8-dione
英文别名
10-hydroxy-9-(4-methoxyphenyl)-3,3,6,6-tetramethyl-4,5,7,9-tetrahydro-2H-acridine-1,8-dione
10-hydroxy-9-(4-methoxyphenyl)-3,3,6,6-tetramethyl-1,2,3,4,5,6,7,8,9,10-decahydroacridine-1,8-dione化学式
CAS
676349-08-9
化学式
C24H29NO4
mdl
——
分子量
395.499
InChiKey
ZLZQLPCXIOVNPM-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):
    4.77
  • 重原子数:
    29.0
  • 可旋转键数:
    2.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    66.84
  • 氢给体数:
    1.0
  • 氢受体数:
    5.0

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    10-hydroxy-9-(4-methoxyphenyl)-3,3,6,6-tetramethyl-1,2,3,4,5,6,7,8,9,10-decahydroacridine-1,8-dione盐酸羟胺 作用下, 以 吡啶 为溶剂, 反应 3.0h, 以81%的产率得到3,3,6,6-tetramethyl-9-(4-methoxyphenyl)-1,2,3,4,5,6,7,8-octahydroacridine-1,8-dione dioxime
    参考文献:
    名称:
    Synthesis and transformations of new 1,2,3,4,5,6,7,8,9,10-decahydroacridine-1,8-dione derivatives
    摘要:
    Reactions of cyclohexane-1,3-diones with amines and aldehydes led to the formation of 1,21,3,4,5,16,7,8,9, 10-decahydroacridine-1,8-diones containing alkylaryl, aryl, and hydroxy substituents in position 10. Transformations of 10-hydroxy-1,2,3,4,5,6,7,8,9,10-decahydroacridine-1,8-diones under oxidation with nitrous acid, reduction with zinc powder, as well as on heating in aprotic solvents and acetic, phosphoric, and polyphosphoric acids, were studied. NMR spectra of 1,2,3,4,5,6,7,8,9,10-decaliydroacridine-1,8-diones having different substituents in positions 9 and 10 were analyzed.
    DOI:
    10.1134/s1070428008080198
  • 作为产物:
    描述:
    4-甲氧基苯甲醛5,5-二甲基-1,3-环己二酮盐酸羟胺 作用下, 以 吡啶 为溶剂, 反应 3.0h, 以89%的产率得到10-hydroxy-9-(4-methoxyphenyl)-3,3,6,6-tetramethyl-1,2,3,4,5,6,7,8,9,10-decahydroacridine-1,8-dione
    参考文献:
    名称:
    Synthesis and transformations of new 1,2,3,4,5,6,7,8,9,10-decahydroacridine-1,8-dione derivatives
    摘要:
    Reactions of cyclohexane-1,3-diones with amines and aldehydes led to the formation of 1,21,3,4,5,16,7,8,9, 10-decahydroacridine-1,8-diones containing alkylaryl, aryl, and hydroxy substituents in position 10. Transformations of 10-hydroxy-1,2,3,4,5,6,7,8,9,10-decahydroacridine-1,8-diones under oxidation with nitrous acid, reduction with zinc powder, as well as on heating in aprotic solvents and acetic, phosphoric, and polyphosphoric acids, were studied. NMR spectra of 1,2,3,4,5,6,7,8,9,10-decaliydroacridine-1,8-diones having different substituents in positions 9 and 10 were analyzed.
    DOI:
    10.1134/s1070428008080198
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文献信息

  • A Novel Cascade Reaction of Aryl Aldoxime with Dimedone Under Microwave Irradiation: The Synthesis of<i>N</i>-Hydroxylacridine
    作者:Shujiang Tu、Chunbao Miao、Yuan Gao、Fang Fang、Qiya Zhuang、Youjian Feng、Daqing Shi
    DOI:10.1055/s-2003-44981
    日期:——
    A novel sequential addition, elimination and cyclization reactions took place when aldoxime and dimedone in glycol was subjected to microwave irradiation and a new type of N-hydroxyl­acridinedione derivatives was obtained in excellent yields (80-95%) within a short reaction time (4-8 min).
    在微波辐照下,乙二醇中的醛和二咪酮发生了新的顺序加成、消除和环化反应,并在很短的反应时间(4-8 分钟)内获得了一种新型的 N-羟基吖啶二酮衍生物,收率极高(80-95%)。
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