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

95%

Reagent Code: #220984
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CAS Number 2924752-26-9

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.1 g/mol
Formula C₁₂H₁₉BN₂O₃
inventory_2 Storage & Handling
Storage -20°C, Inert Gas

description Product Description

Used in organic synthesis as a pyrazole-based building block for cross-coupling reactions, particularly in Suzuki-Miyaura coupling, enabling the formation of biaryl or heteroaryl compounds. Its boronate ester group facilitates carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research for constructing complex molecules. The oxetane ring adds polarity and metabolic stability, often beneficial in drug design for improving pharmacokinetic properties. Commonly employed in medicinal chemistry for lead optimization and library synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,820.00
inventory 250mg
10-20 days ฿9,310.00
inventory 1g
10-20 days ฿24,200.00
1-(Oxetan-3-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
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Used in organic synthesis as a pyrazole-based building block for cross-coupling reactions, particularly in Suzuki-Miyaura coupling, enabling the formation of biaryl or heteroaryl compounds. Its boronate ester group facilitates carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research for constructing complex molecules. The oxetane ring adds polarity and metabolic stability, often beneficial in drug design for improving pharmacokinetic properties. Commonly employed in me

Used in organic synthesis as a pyrazole-based building block for cross-coupling reactions, particularly in Suzuki-Miyaura coupling, enabling the formation of biaryl or heteroaryl compounds. Its boronate ester group facilitates carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research for constructing complex molecules. The oxetane ring adds polarity and metabolic stability, often beneficial in drug design for improving pharmacokinetic properties. Commonly employed in medicinal chemistry for lead optimization and library synthesis.

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