2-(4-Bromobutyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

95%

Reagent Code: #130984
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CAS Number 124215-50-5

science Other reagents with same CAS 124215-50-5

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scatter_plot Molecular Information
Weight 262.98 g/mol
Formula C₁₀H₂₀BBrO₂
badge Registry Numbers
MDL Number MFCD22419948
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used primarily as an intermediate in organic synthesis, especially in cross-coupling reactions such as Suzuki-Miyaura coupling. Its bromobutyl group enables alkylation or chain extension, while the dioxaborolane moiety acts as a protected form of boronic acid, facilitating the formation of carbon-carbon bonds. Commonly employed in the preparation of functionalized organic molecules for pharmaceuticals, agrochemicals, and advanced materials. Stable and easy to handle, it allows for selective transformations in multi-step syntheses.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿13,300.00
inventory 250mg
10-20 days ฿4,990.00

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2-(4-Bromobutyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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Used primarily as an intermediate in organic synthesis, especially in cross-coupling reactions such as Suzuki-Miyaura coupling. Its bromobutyl group enables alkylation or chain extension, while the dioxaborolane moiety acts as a protected form of boronic acid, facilitating the formation of carbon-carbon bonds. Commonly employed in the preparation of functionalized organic molecules for pharmaceuticals, agrochemicals, and advanced materials. Stable and easy to handle, it allows for selective transformatio

Used primarily as an intermediate in organic synthesis, especially in cross-coupling reactions such as Suzuki-Miyaura coupling. Its bromobutyl group enables alkylation or chain extension, while the dioxaborolane moiety acts as a protected form of boronic acid, facilitating the formation of carbon-carbon bonds. Commonly employed in the preparation of functionalized organic molecules for pharmaceuticals, agrochemicals, and advanced materials. Stable and easy to handle, it allows for selective transformations in multi-step syntheses.

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