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CF0024

Sigma-Aldrich

4-Ethoxycarbonylphenoxytetrafluoroethyl trimethylsilane

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About This Item

线性分子式:
C14H18F4O3Si
CAS号:
1836233-51-2
MDL號碼:
MFCD31618506
分類程式碼代碼:
12352101

形狀

liquid

反應適用性

reaction type: C-C Bond Formation

應用

After being activated with silicophilic activators, like fluorides, alkoxides or carboxylates, 4-ethoxycarbonylphenoxytetrafluoroethyl trimethylsilane serves as a nucleophilic source of the 4-ethoxycarbonylphenoxytetrafluoroethyl moiety in reaction with electrophiles such as aromatic aldehydes. The ester group can be used to further build up molecular complexity.

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其他說明

Technology Spotlight: Fluoroalkylation: Expansion of Togni Reagents

法律資訊

Product of CF Plus Chemicals.

儲存類別代碼

10 - Combustible liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

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分析证书(COA)

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Fluoroalkylation: Expansion of Togni Reagents

The fluoroalkylation toolbox now includes Togni reagents, hypervalent iodine perfluoroalkylation reagents, fluoroalkyl bromides, silanes, carboxylates, and sulfonyl fluorides for late stage fluoroalkylation.

Fluoroalkylation: Expansion of Togni Reagents

The fluoroalkylation toolbox now includes Togni reagents, hypervalent iodine perfluoroalkylation reagents, fluoroalkyl bromides, silanes, carboxylates, and sulfonyl fluorides for late stage fluoroalkylation.

Fluoroalkylation: Expansion of Togni Reagents

The fluoroalkylation toolbox now includes Togni reagents, hypervalent iodine perfluoroalkylation reagents, fluoroalkyl bromides, silanes, carboxylates, and sulfonyl fluorides for late stage fluoroalkylation.

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