2-Bromo-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazole

95%

Reagent Code: #89809
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CAS Number 1402166-32-8

science Other reagents with same CAS 1402166-32-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 289.99 g/mol
Formula C₉H₁₃BBrNO₂S
badge Registry Numbers
MDL Number MFCD13181957
thermostat Physical Properties
Boiling Point 341.0±15.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.44±0.1 g/cm3(Predicted)
Storage -20°C, sealed, dry

description Product Description

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical research and drug development. It is often employed in the synthesis of thiazole-containing compounds, which are significant in medicinal chemistry due to their biological activity. Additionally, it serves as a building block in material science for creating advanced organic materials with specific electronic or optical properties. Its stability and reactivity make it a preferred choice for introducing thiazole moieties into target molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,752.00
inventory 25mg
10-20 days ฿1,053.00
inventory 100mg
10-20 days ฿2,115.00

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2-Bromo-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazole
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This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical research and drug development. It is often employed in the synthesis of thiazole-containing compounds, which are significant in medicinal chemistry due to their biological activity. Additionally, it serves as a building block in material science for creating

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical research and drug development. It is often employed in the synthesis of thiazole-containing compounds, which are significant in medicinal chemistry due to their biological activity. Additionally, it serves as a building block in material science for creating advanced organic materials with specific electronic or optical properties. Its stability and reactivity make it a preferred choice for introducing thiazole moieties into target molecules.

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