2-(3-Bromo-2-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

98%

Reagent Code: #129906
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CAS Number 2057523-47-2

science Other reagents with same CAS 2057523-47-2

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scatter_plot Molecular Information
Weight 297 g/mol
Formula C₁₃H₁₈BBrO₂
badge Registry Numbers
MDL Number MFCD29088138
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used primarily as a reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its boronate ester group readily transmetallates with palladium catalysts, making it valuable for constructing biaryl and heterobiaryl compounds in pharmaceuticals, agrochemicals, and advanced materials. The bromo substituent allows for sequential functionalization, supporting multi-step syntheses where selective reactivity is required. Stable and easy to handle, it serves as a versatile building block in medicinal chemistry and drug development.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿11,400.00
inventory 250mg
10-20 days ฿4,280.00

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2-(3-Bromo-2-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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Used primarily as a reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its boronate ester group readily transmetallates with palladium catalysts, making it valuable for constructing biaryl and heterobiaryl compounds in pharmaceuticals, agrochemicals, and advanced materials. The bromo substituent allows for sequential functionalization, supporting multi-step syntheses where selective reactivity is required. Stable and easy to handle, it

Used primarily as a reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its boronate ester group readily transmetallates with palladium catalysts, making it valuable for constructing biaryl and heterobiaryl compounds in pharmaceuticals, agrochemicals, and advanced materials. The bromo substituent allows for sequential functionalization, supporting multi-step syntheses where selective reactivity is required. Stable and easy to handle, it serves as a versatile building block in medicinal chemistry and drug development.

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