4-Amino-2-(pyridin-2-yl)pyrimidine-5-boronic acid pinacol ester

95%

Reagent Code: #60868
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CAS Number 2223054-09-7

science Other reagents with same CAS 2223054-09-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 316.16324 g/mol
Formula C₁₅H₂₁BN₄O₃
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is widely utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronic ester group makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of complex molecules in pharmaceutical and material science research. It is often employed in the development of drug candidates, where it serves as a key intermediate for introducing pyrimidine and pyridine moieties into target structures. Additionally, its stability and reactivity make it suitable for use in combinatorial chemistry and high-throughput screening processes.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿46,782.00
inventory 5mg
10-20 days ฿16,182.00

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4-Amino-2-(pyridin-2-yl)pyrimidine-5-boronic acid pinacol ester
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This compound is widely utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronic ester group makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of complex molecules in pharmaceutical and material science research. It is often employed in the development of drug candidates, where it serves as a key intermediate for introducing pyrimidine and pyridine moieties into target structures. Additionally, its stability

This compound is widely utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronic ester group makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of complex molecules in pharmaceutical and material science research. It is often employed in the development of drug candidates, where it serves as a key intermediate for introducing pyrimidine and pyridine moieties into target structures. Additionally, its stability and reactivity make it suitable for use in combinatorial chemistry and high-throughput screening processes.

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