2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

97%

Reagent Code: #174553
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CAS Number 1003298-87-0

science Other reagents with same CAS 1003298-87-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.96 g/mol
Formula C₁₂H₁₅BCl₂O₃
badge Registry Numbers
MDL Number MFCD20526385
inventory_2 Storage & Handling
Storage Room temperature, stored in inert gas

description Product Description

Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, allowing for the construction of biaryl and heterobiaryl structures. Its phenolic hydroxyl group provides a handle for further functionalization or protection, making it valuable in multi-step synthetic routes. Due to its stability and reactivity, it is preferred in the preparation of functional materials, including liquid crystals and organic electronic materials.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿297.00
inventory 1g
10-20 days ฿731.50
inventory 5g
10-20 days ฿4,140.00

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2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
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Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, allowing for the construction of biaryl and heterobiaryl structures. Its phenolic hydroxyl group provides a handle for further functionalization or protection, making it valuable in multi-step synthetic routes.

Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, allowing for the construction of biaryl and heterobiaryl structures. Its phenolic hydroxyl group provides a handle for further functionalization or protection, making it valuable in multi-step synthetic routes. Due to its stability and reactivity, it is preferred in the preparation of functional materials, including liquid crystals and organic electronic materials.

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