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

95%

Reagent Code: #241702
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CAS Number 1029715-63-6

science Other reagents with same CAS 1029715-63-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.13 g/mol
Formula C₁₃H₂₁BN₂O₃
badge Registry Numbers
MDL Number MFCD18383269
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex pyrazole-containing compounds. Its boronate ester group facilitates carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research for building bioactive molecules. Commonly employed in the development of drug candidates where pyrazole scaffolds are present, particularly in anti-inflammatory, antiviral, and kinase inhibitor programs. Its tetrahydrofuran ring adds structural diversity, enhancing solubility and binding affinity in target molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿610.00
inventory 250mg
10-20 days ฿564.00
inventory 1g
10-20 days ฿3,710.00
inventory 5g
10-20 days ฿12,280.00

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1-(Tetrahydrofuran-3-yl)-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 synthesis of complex pyrazole-containing compounds. Its boronate ester group facilitates carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research for building bioactive molecules. Commonly employed in the development of drug candidates where pyrazole scaffolds are present, particularly in anti-inflammatory, antiviral, and kinase inhibitor programs. Its tetrahydrofu

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex pyrazole-containing compounds. Its boronate ester group facilitates carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research for building bioactive molecules. Commonly employed in the development of drug candidates where pyrazole scaffolds are present, particularly in anti-inflammatory, antiviral, and kinase inhibitor programs. Its tetrahydrofuran ring adds structural diversity, enhancing solubility and binding affinity in target molecules.

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