1-(Phenylsulfonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

97%

Reagent Code: #225444
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CAS Number 1073372-04-9

science Other reagents with same CAS 1073372-04-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 334.2 g/mol
Formula C₁₅H₁₉BN₂O₄S
thermostat Physical Properties
Melting Point 125-130°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or heteroaryl halides, making it valuable for constructing complex pyrazole-containing molecules. Commonly employed in the development of bioactive compounds, including kinase inhibitors and other therapeutic agents. Its sulfonyl group enhances stability and influences electronic properties, improving reaction efficiency and selectivity in heterocyclic chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,460.00
inventory 1g
10-20 days ฿3,420.00
inventory 5g
10-20 days ฿12,600.00
inventory 25g
10-20 days ฿40,700.00
1-(Phenylsulfonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or heteroaryl halides, making it valuable for constructing complex pyrazole-containing molecules. Commonly employed in the development of bioactive compounds, including kinase inhibitors and other therapeutic agents. Its sulfonyl group enhances stability an

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or heteroaryl halides, making it valuable for constructing complex pyrazole-containing molecules. Commonly employed in the development of bioactive compounds, including kinase inhibitors and other therapeutic agents. Its sulfonyl group enhances stability and influences electronic properties, improving reaction efficiency and selectivity in heterocyclic chemistry.

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