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Merck

903981

Sigma-Aldrich

2,3,7,8-Tetrafluorothianthrene-S-oxide

≥95%

别名:

2,3,7,8-Tetrafluorothianthrene-5-oxide, Fluorinated sulfoxide-based thianthrene reagent, Ritter C-H functionalization linchpin, TFT S-oxide, TFT-reagent

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About This Item

经验公式(希尔记法):
C12H4F4OS2
分子量:
304.28
MDL號碼:
分類程式碼代碼:
12352101
NACRES:
NA.22

化驗

≥95%

形狀

solid

mp

253 °C

官能基

fluoro
sulfoxide
thioether

儲存溫度

−20°C

SMILES 字串

Fc1cc2c(cc1F)Sc3c(cc(c(c3)F)F)[S]2=O

InChI

1S/C12H4F4OS2/c13-5-1-9-11(3-7(5)15)19(17)12-4-8(16)6(14)2-10(12)18-9/h1-4H

InChI 密鑰

FJNMYEBXFNFTBJ-UHFFFAOYSA-N

應用

2,3,7,8-Tetrafluorothianthrene-S-oxide (TFT S-oxide) is a fluorinated sulfoxide-based thianthrene reagent for late-stage C-H functionalization. Developed by the Ritter Lab, C-H functionalization by thianthrenation with TFT S-oxide proceeds with >99% selectivity and furnishes functionalized arenes serving as synthetic linchpins for further participation in diverse transformations.
The nonfluorinated thianthrene S-oxide is also available as catalog# 903973 for all arenes more electron-rich than anisole.

法律資訊

Patent Application EP18204755.5
This product is manufactured pursuant to a license with Studiengesellschaft Kohle mbH

相關產品

产品编号
说明
价格

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Florian Berger et al.
Nature, 567(7747), 223-228 (2019-03-15)
Direct C-H functionalization can quickly increase useful structural and functional molecular complexity1-3. Site selectivity can sometimes be achieved through appropriate directing groups or substitution patterns1-4-in the absence of such functionality, most aromatic C-H functionalization reactions provide more than one product

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