5-(5-Pyrimidyl)thiazole-4-boronic acid pinacol ester

95%

Reagent Code: #90817
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CAS Number 2223039-32-3

science Other reagents with same CAS 2223039-32-3

blur_circular Chemical Specifications

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Weight 307.17632 g/mol
Formula C₁₃H₁₈BN₃O₃S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Used in organic synthesis as a key intermediate for the preparation of various heterocyclic compounds, particularly those featuring pyrimidine and thiazole structures. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. This makes it essential in the development of pharmaceuticals, agrochemicals, and materials science. Its boronic ester group allows for selective functionalization, facilitating the creation of complex molecules with potential biological activity. Often employed in the synthesis of drug candidates targeting specific enzymes or receptors.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿24,300.00
inventory 5mg
10-20 days ฿8,280.00

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5-(5-Pyrimidyl)thiazole-4-boronic acid pinacol ester
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Used in organic synthesis as a key intermediate for the preparation of various heterocyclic compounds, particularly those featuring pyrimidine and thiazole structures. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. This makes it essential in the development of pharmaceuticals, agrochemicals, and materials science. Its boronic ester group allows for selective functionalization, facilitating the creation of complex molecules with poten

Used in organic synthesis as a key intermediate for the preparation of various heterocyclic compounds, particularly those featuring pyrimidine and thiazole structures. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. This makes it essential in the development of pharmaceuticals, agrochemicals, and materials science. Its boronic ester group allows for selective functionalization, facilitating the creation of complex molecules with potential biological activity. Often employed in the synthesis of drug candidates targeting specific enzymes or receptors.

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