跳转至内容
Merck
CN
所有图片(1)

文件

安全信息

920223

Sigma-Aldrich

3,6-Di-tert-butyl-9-(2,6-dimethylphenyl)-10-(4-(trifluoromethyl)phenyl)acridin-10-ium tetrafluoroborate

≥95%

登录查看公司和协议定价
所有图片(1)
经验公式（希尔记法）:
C36H37BF7N
CAS号:
2363740-69-4
分子量:
627.49
NACRES:
NA.22

质量水平

100

检测方案

≥95%

形式

powder or crystals

反应适用性

reaction type: Photocatalysis
reagent type: catalyst

储存温度

−20°C

相关类别

应用

3,6-Di-tert-butyl-9-(2,6-dimethylphenyl)-10-(4-(trifluoromethyl)phenyl)acridin-10-ium tetrafluoroborate is a robust acridinium-based photocatalyst reported by Nicewicz and coworkers as an alternative to transition-metal-based photocatalysts with higher chemical stability and attenuated redox potential.

Product can be used with our line of photoreactors: Including Penn PhD (Z744035) & SynLED 2.0 (Z744080)

其他说明

Nucleophilic Aromatic Substitution of Unactivated Fluoroarenes Enabled by Organic Photoredox Catalysis

相关产品

产品编号
说明
价格

794171

9-间二甲基-10-甲基吖啶鎓四氟硼酸盐

793221

9-均三苯-10-苯吖啶四氟硼酸盐

747610

9-均三甲基-10-甲基吖啶高氯酸盐, 95%

900421

9-均三苯-3,6-二- 叔 -丁基-10-苯基吖啶四氟硼酸盐, ≥95%

900693

9-均三甲苯基-1,3,6,8-四甲氧基-10-苯基吖啶-10-四氟硼酸铵, 95%

900694

10-（3,5-二甲氧基苯基）-9-均三甲苯基-1,3,6,8-四甲氧基吖啶-10-溴四氟硼酸盐, ≥93%

909033

2,7-Dibromo-9-mesityl-10-methylacridinium tetrafluoroborate

909181

2,7-Dimethyl-9-mesityl-10-methylacridinium tetrafluoroborate

909254

2,7-Difluoro-9-mesityl-10-methylacridinium tetrafluoroborate

909319

2,7-Dibromo-10-methylacridone, ≥95%

909327

2,7-Dimethoxy-9-mesityl-10-methylacridinium tetrafluoroborate

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

新产品

分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ （Lot或Batch）字后找到。

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

Vincent A Pistritto et al.
Journal of the American Chemical Society, 142(40), 17187-17194 (2020-09-29)
Nucleophilic aromatic substitution (SNAr) is a classical reaction with well-known reactivity toward electron-poor fluoroarenes. However, electron-neutral and electron-rich fluoro(hetero)arenes are considerably underrepresented. Herein, we present a method for the nucleophilic defluorination of unactivated fluoroarenes enabled by cation radical-accelerated nucleophilic aromatic

我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门