所有图片(1)

主要文件

920223

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

Name: 3,6-Di-<I>tert</I>-butyl-9-(2,6-dimethylphenyl)-10-(4-(trifluoromethyl)phenyl)acridin-10-ium tetrafluoroborate
Brand: ALDRICH

≥95%

登录查看公司和协议定价

所有图片(1)

About This Item

经验公式（希尔记法）:

C₃₆H₃₇BF₇N

CAS号:

2363740-69-4

分子量:

627.49

分類程式碼代碼:

12352103

NACRES:

NA.22

推荐产品

Slide 1 of 10

1 of 10

Sigma-Aldrich

793876

9-均三甲苯基-2,7-二甲基-10-苯基吖啶四氟硼酸盐

Sigma-Aldrich

900421

9-均三苯-3,6-二- 叔 -丁基-10-苯基吖啶四氟硼酸盐

Sigma-Aldrich

794171

9-间二甲基-10-甲基吖啶鎓四氟硼酸盐

Sigma-Aldrich

909033

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

Sigma-Aldrich

Z744035

Penn PhD Photoreactor M2

Sigma-Aldrich

909181

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

Sigma-Aldrich

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

R251437

2,6-DI-TERT-BUTYL-4-(PYRIDIN-4-YL)PYRYLIUM 4-(2,6-DI-TERT-BUTYLPYRYLIUM-4-YL)PYRIDINIUM TETRAFLUOROBORATE

Sigma-Aldrich

05-829

抗-α-微管蛋白抗体，克隆DM1A

Sigma-Aldrich

909254

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

品質等級

100

化驗

≥95%

形狀

powder or crystals

反應適用性

reaction type: Photocatalysis
reagent type: catalyst

儲存溫度

−20°C

應用

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)

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

从最新的版本中选择一种：

分析证书(COA)

Lot/Batch Number

抱歉，我们目前尚未线上提供该产品的COA。

如需帮助，请联系客户支持

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

Nucleophilic Aromatic Substitution of Unactivated Fluoroarenes Enabled by Organic Photoredox Catalysis.

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

主要文件

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