4,4,5,5-Tetramethyl-2-(4-((trifluoromethyl)sulfonyl)phenyl)-1,3,2-dioxaborolane

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Reagent Code: #244476
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CAS Number 648904-89-6

science Other reagents with same CAS 648904-89-6

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scatter_plot Molecular Information
Weight 336.13 g/mol
Formula C₁₃H₁₆BF₃O₄S
badge Registry Numbers
MDL Number MFCD28969495
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Widely used in cross-coupling reactions, this compound serves as a key boronic ester reagent in Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its electron-deficient aryl group enhances reactivity and stability, making it valuable for constructing complex aromatic systems. It is particularly useful in late-stage functionalization due to its tolerance of various functional groups and compatibility with palladium catalysts. Additionally, it acts as a building block in materials science for designing organic electronic materials and conjugated polymers.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,450.00
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4,4,5,5-Tetramethyl-2-(4-((trifluoromethyl)sulfonyl)phenyl)-1,3,2-dioxaborolane
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Widely used in cross-coupling reactions, this compound serves as a key boronic ester reagent in Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its electron-deficient aryl group enhances reactivity and stability, making it valuable for constructing complex aromatic systems. It is particularly useful in late-stage functionalization due to its tolerance of various functional groups and compatibility with palladium catalysts. Additionally, it acts as a building block in materials science for designing organic electronic materials and conjugated polymers.
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