Ethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate

95%

Reagent Code: #182516
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CAS Number 195062-62-5

science Other reagents with same CAS 195062-62-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.14 g/mol
Formula C₁₅H₂₁BO₄
thermostat Physical Properties
Boiling Point 370.2°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for forming carbon-carbon bonds in organic synthesis. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or vinyl halides, making it valuable in the preparation of complex aromatic systems. It is especially useful in pharmaceutical and agrochemical industries for constructing biaryl motifs found in active ingredients. The ester functionality allows further transformations, such as hydrolysis to carboxylic acids or reduction to alcohols, enabling diverse molecular diversification. Its stability and reactivity profile make it a preferred reagent in both research and industrial settings for late-stage functionalization.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,330.00
inventory 10g
10-20 days ฿2,640.00
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Ethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
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Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for forming carbon-carbon bonds in organic synthesis. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or vinyl halides, making it valuable in the preparation of complex aromatic systems. It is especially useful in pharmaceutical and agrochemical industries for constructing biaryl motifs found in active ingredients. The ester functionality allows further transformations, such as hydrolysis to carboxylic acids or reduction to alcohols, enabling diverse molecular diversification. Its stability and reactivity profile make it a preferred reagent in both research and industrial settings for late-stage functionalization.
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