(6-(thiazol-4-yl)pyridin-3-yl)boronic acid

95%

Reagent Code: #89373
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CAS Number 1264511-59-2

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.02938 g/mol
Formula C₈H₇BN₂O₂S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. The boronic acid group enables the formation of carbon-carbon bonds, making it valuable for creating biologically active compounds, such as drug candidates targeting specific enzymes or receptors. Its thiazole and pyridine moieties contribute to its potential in designing molecules with enhanced binding affinity and selectivity, often explored in medicinal chemistry for treating diseases like cancer or infections. Additionally, it may be utilized in material science for developing functionalized polymers or advanced materials with tailored properties.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿86,000.00
100mg
10-20 days ฿258,000.00
(6-(thiazol-4-yl)pyridin-3-yl)boronic acid
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This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. The boronic acid group enables the formation of carbon-carbon bonds, making it valuable for creating biologically active compounds, such as drug candidates targeting specific enzymes or receptors. Its thiazole and pyridine moieties contribute to its potential in designing mo

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. The boronic acid group enables the formation of carbon-carbon bonds, making it valuable for creating biologically active compounds, such as drug candidates targeting specific enzymes or receptors. Its thiazole and pyridine moieties contribute to its potential in designing molecules with enhanced binding affinity and selectivity, often explored in medicinal chemistry for treating diseases like cancer or infections. Additionally, it may be utilized in material science for developing functionalized polymers or advanced materials with tailored properties.

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