(4-((4-((tert-Butyldimethylsilyl)oxy)piperidin- 1-yl)sulfonyl)-2-fluorophenyl)boronic acid

98%

Reagent Code: #89185
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CAS Number 1704096-28-5

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Weight 417.38 g/mol
Formula C₁₇H₂₉BFNO₅SSi
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and advanced materials. The tert-butyldimethylsilyl (TBDMS) protecting group enhances its stability during reactions, allowing for selective transformations. It is often employed in medicinal chemistry for the development of drug candidates, especially in the modification of aromatic compounds. Additionally, its fluorophenyl moiety can influence the electronic properties of the final product, making it useful in the design of bioactive molecules.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿50,210.00
(4-((4-((tert-Butyldimethylsilyl)oxy)piperidin- 1-yl)sulfonyl)-2-fluorophenyl)boronic acid
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and advanced materials. The tert-butyldimethylsilyl (TBDMS) protecting group enhances its stability during reactions, allowing for selective transformations. It is often employed in medicinal chemistry for the development of drug candidates, especially in the modification of aromatic compounds. Additionally, its fluorophenyl moiety can influence the electronic properties of the final product, making it useful in the design of bioactive molecules.
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