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

95%

Reagent Code: #90682
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CAS Number 1440520-87-5

science Other reagents with same CAS 1440520-87-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 208.07 g/mol
Formula C₁₀H₁₇BN₂O₂
badge Registry Numbers
MDL Number MFCD27977041
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of complex molecules, often in pharmaceutical research and development. Its boronate ester group makes it valuable in Suzuki-Miyaura coupling reactions, enabling the formation of carbon-carbon bonds. This is crucial for constructing biologically active compounds, including potential drug candidates. Additionally, it is employed in the synthesis of heterocyclic compounds, which are widely used in medicinal chemistry for their diverse pharmacological properties. Its stability and reactivity make it a preferred choice for designing and synthesizing novel organic molecules.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿8,280.00
inventory 100mg
10-20 days ฿16,992.00
inventory 250mg
10-20 days ฿35,892.00

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4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of complex molecules, often in pharmaceutical research and development. Its boronate ester group makes it valuable in Suzuki-Miyaura coupling reactions, enabling the formation of carbon-carbon bonds. This is crucial for constructing biologically active compounds, including potential drug candidates. Additionally, it is employed in the synthesis of heterocyclic compounds, which are widely used in medicinal chemistry for their diverse pharmacological properties. Its stability and reactivity make it a preferred choice for designing and synthesizing novel organic molecules.
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