2-Ethoxy-pyrimidine-5-boronic acid pinacol ester

98%

Reagent Code: #183461
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CAS Number 1147105-68-7

science Other reagents with same CAS 1147105-68-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.1300 g/mol
Formula C₁₄H₂₁BO₃
badge Registry Numbers
MDL Number MFCD09027075
thermostat Physical Properties
Boiling Point 336.9±25.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.01±0.1g/ml(Predicted)
Storage 2-8℃, dry, sealed

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex pyrimidine derivatives in pharmaceutical and agrochemical research. Its boronic ester group facilitates efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery for building bioactive molecules. Commonly employed in the development of kinase inhibitors and other therapeutic agents where pyrimidine scaffolds are essential. Also applied in materials science for constructing functional organic compounds with tailored electronic properties. The stability of the pinacol ester enhances storage and handling in multi-step syntheses.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,960.00
inventory 5g
10-20 days ฿14,860.00
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2-Ethoxy-pyrimidine-5-boronic acid pinacol ester
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex pyrimidine derivatives in pharmaceutical and agrochemical research. Its boronic ester group facilitates efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery for building bioactive molecules. Commonly employed in the development of kinase inhibitors and other therapeutic agents where pyrimidine scaffolds are essential. Also applied in materials science for

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex pyrimidine derivatives in pharmaceutical and agrochemical research. Its boronic ester group facilitates efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery for building bioactive molecules. Commonly employed in the development of kinase inhibitors and other therapeutic agents where pyrimidine scaffolds are essential. Also applied in materials science for constructing functional organic compounds with tailored electronic properties. The stability of the pinacol ester enhances storage and handling in multi-step syntheses.

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