2-[[(tert-Butyldimethylsilyl)oxy]methyl]-6-chlorophenylboronic Acid Pinacol Ester

95%

Reagent Code: #89768

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 382.81 g/mol
Formula C₁₉H₃₂ClO₃BSi
badge Registry Numbers
MDL Number MFCD28101624
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic ester group facilitates the coupling with aryl or vinyl halides, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butyldimethylsilyl (TBDMS) protecting group enhances stability during reactions, allowing for selective transformations. Commonly applied in the synthesis of biologically active compounds, such as drug candidates, where precise molecular architecture is crucial. Also utilized in material science for creating advanced polymers and functionalized materials.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿18,576.00
inventory 1g
10-20 days ฿49,230.00

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2-[[(tert-Butyldimethylsilyl)oxy]methyl]-6-chlorophenylboronic Acid Pinacol Ester
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Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic ester group facilitates the coupling with aryl or vinyl halides, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butyldimethylsilyl (TBDMS) protecting group enhances stability during reactions, allowing for selective transformations. Commonly applied in the synthesis of biologically active

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic ester group facilitates the coupling with aryl or vinyl halides, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butyldimethylsilyl (TBDMS) protecting group enhances stability during reactions, allowing for selective transformations. Commonly applied in the synthesis of biologically active compounds, such as drug candidates, where precise molecular architecture is crucial. Also utilized in material science for creating advanced polymers and functionalized materials.

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