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

97%

Reagent Code: #204154
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CAS Number 1616930-45-0

science Other reagents with same CAS 1616930-45-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 266.10 g/mol
Formula C₁₂H₁₉BN₂O₄
badge Registry Numbers
MDL Number MFCD31743612
inventory_2 Storage & Handling
Storage -20°C, Sealed, Dry

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex pyrazole derivatives with pharmaceutical relevance. Its boronate ester group facilitates carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and development of bioactive molecules. Commonly employed in the preparation of kinase inhibitors and other therapeutic agents where the pyrazole core is essential for biological activity. Also applied in materials science for constructing conjugated systems in organic electronics.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿5,110.00
250mg
10-20 days ฿10,230.00
1g
10-20 days ฿25,600.00
Methyl 1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-3-carboxylate
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex pyrazole derivatives with pharmaceutical relevance. Its boronate ester group facilitates carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and development of bioactive molecules. Commonly employed in the preparation of kinase inhibitors and other therapeutic agents where the pyrazole core is essential for biological activity. Also applied in materials science for

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex pyrazole derivatives with pharmaceutical relevance. Its boronate ester group facilitates carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and development of bioactive molecules. Commonly employed in the preparation of kinase inhibitors and other therapeutic agents where the pyrazole core is essential for biological activity. Also applied in materials science for constructing conjugated systems in organic electronics.

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