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

10-(3-ethoxyphenyl)anthracene | 1362419-05-3

中文名称
——
中文别名
——
英文名称
10-(3-ethoxyphenyl)anthracene
英文别名
9-(3-Ethoxyphenyl)anthracene
10-(3-ethoxyphenyl)anthracene化学式
CAS
1362419-05-3
化学式
C22H18O
mdl
——
分子量
298.384
InChiKey
QTDDKSCJWAPWEV-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):
    6.3
  • 重原子数:
    23
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    9-溴蒽3-乙氧基苯硼酸 在 C70H40Cl2F68N2O6Pd2四丁基溴化铵potassium carbonate 作用下, 以 为溶剂, 反应 0.08h, 以89%的产率得到10-(3-ethoxyphenyl)anthracene
    参考文献:
    名称:
    Fluorous Oxime Palladacycle: A Precatalyst for Carbon–Carbon Coupling Reactions in Aqueous and Organic Medium
    摘要:
    To facilitate precatalyst recovery and reuse, we have developed a fluorous, oxime-based palladacycle 1 and demonstrated that it is a very efficient and versatile precatalyst for a wide range of carbon carbon bond formation reactions (Suzuki-Miyaura, Sonogashira, Stille, Heck, Glaser-type, and Kumada) in either aqueous or organic medium under microwave irradiation. Palladacycle 1 could be recovered through F-SPE in various coupling reactions with recovery ranging from 84 to 95% for the first cycle. Inductively coupled plasma optical emission spectrometry (ICP-OES) analyses of the Pd content in the crude product from each class of transformation indicated extremely low levels of leaching and the palladacycle could be reused four to five times without significant loss of activity.
    DOI:
    10.1021/jo202482h
点击查看最新优质反应信息

文献信息

  • Fluorous Oxime Palladacycle: A Precatalyst for Carbon–Carbon Coupling Reactions in Aqueous and Organic Medium
    作者:Woen Susanto、Chi-Yuan Chu、Wei Jie Ang、Tzyy-Chao Chou、Lee-Chiang Lo、Yulin Lam
    DOI:10.1021/jo202482h
    日期:2012.3.16
    To facilitate precatalyst recovery and reuse, we have developed a fluorous, oxime-based palladacycle 1 and demonstrated that it is a very efficient and versatile precatalyst for a wide range of carbon carbon bond formation reactions (Suzuki-Miyaura, Sonogashira, Stille, Heck, Glaser-type, and Kumada) in either aqueous or organic medium under microwave irradiation. Palladacycle 1 could be recovered through F-SPE in various coupling reactions with recovery ranging from 84 to 95% for the first cycle. Inductively coupled plasma optical emission spectrometry (ICP-OES) analyses of the Pd content in the crude product from each class of transformation indicated extremely low levels of leaching and the palladacycle could be reused four to five times without significant loss of activity.
查看更多

同类化合物

金不换萘酚 金不换素 蒽,9,10-二[4-(2,2-二苯基乙烯基)苯基]- 萘并[2,3-c]呋喃-1,3-二酮,6-甲氧基-4-(4-甲氧苯基)- 萘并[2,3-c]呋喃-1(3H)-酮,7-羟基-4-(3-甲氧苯基)- 萘并[2,3-c]呋喃-1(3H)-酮,4-(2-氟苯基)-7-(苯基甲氧基)- 苯氧基-9苯基-10蒽 苯基-(10-苯基蒽-9-基)甲酮 红荧烯 甲基7-苯基二苯并(A,J)蒽-14-羧酸酯 甲基10-苯基-9-蒽羧酸酯 爵床脂素 B 爵床脂素 A 木酚素J1(P) 昔土米霉素 新爵床素 B 拒食胺 大麻酰胺 地蒽酚10,10'-二聚体 四去氢鬼臼毒素 叶下珠醇抑制剂A 二甲基4-(3,4-二甲氧苯基)-1-羟基-5,6,7-三甲氧基萘-2,3-二甲酸基酯 二叶草素 [4-(3,10-二羟基蒽-9-基)苯基]乙酸乙酸酯 [4-(10-羟基蒽-9-基)苯基]乙酸乙酸酯 [2-甲氧基-10-(4-甲氧基苯基)蒽-9-基]乙酸酯 [10-羟基-5-(10-羟基-7,9-二甲氧基-3-甲基-3,4-二氢-1H-苯并[g]异苯并吡喃-5-基)-7,9-二甲氧基-3-甲基-3,4-二氢-1H-苯并[g]异苯并吡喃-4-基]乙酸酯 [10-(9,9-二甲基芴-2-基)蒽-9-基]硼酸 [10-(4-叔丁基苯基)蒽-9-基]硼酸 B-[10-(4-苯基-1-萘基)-9-蒽基]硼酸 B-(9,10-二苯基-2-蒽)硼酸 9.10-二(3',5'-二羧基苯基)蒽 9-萘-1-基-10-(4-苯基苯基)蒽 9-苯基蒽 9-苯基-10-苯乙炔基菲 9-苯基-10-硝基蒽 9-苯基-10-(苯基乙炔基)蒽 9-苯基-10-(4-三苯胺)蒽 9-苯基-1,2,3,4-四氢蒽 9-羟基-10-甲氧基-5-(3,4,5-三甲氧基苯基)-8H-[2]苯并呋喃并[6,5-f][1,3]苯并二氧戊环-6-酮 9-碘-10-(10-碘蒽-9-基)蒽 9-甲氧基-10-苯基蒽 9-甲基-10-苯基菲 9-溴-10-苯基蒽 9-溴-10-[4-(2-萘基)苯基]蒽 9-溴-10-[3-(2-萘基)苯基]蒽 9-溴-10-[3-(10-溴蒽-9-基)-5-甲基苯基]蒽 9-溴-10-[1,1':3',1''-三联苯]-5'-基蒽 9-溴-10-(4-苯基萘-1-基)蒽 9-溴-10-(2-萘基)蒽