Thiazole-5-boronic Acid Pinacol Ester

≥95%

Reagent Code: #91132
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CAS Number 1086111-09-2

science Other reagents with same CAS 1086111-09-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.09 g/mol
Formula C₉H₁₄NO₂SB
badge Registry Numbers
MDL Number MFCD10697440
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Thiazole-5-boronic Acid Pinacol Ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a preferred reagent for introducing thiazole moieties into complex molecules, enhancing their biological activity or functional properties. Additionally, it is employed in the development of heterocyclic compounds, which are crucial in drug discovery and material science. Its versatility also extends to the synthesis of organic electronic materials, where thiazole derivatives play a role in improving performance.

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Test Parameter Specification
Appearance Off-White Powder
Purity (%) 95-100
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,377.00
inventory 5g
10-20 days ฿7,767.00
inventory 1g
10-20 days ฿2,853.00

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Thiazole-5-boronic Acid Pinacol Ester
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Thiazole-5-boronic Acid Pinacol Ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a preferred reagent for introducing thiazole moieties into complex molecules, enhancing their biological activity or functional properties. Additionally, it is employed in the developm

Thiazole-5-boronic Acid Pinacol Ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a preferred reagent for introducing thiazole moieties into complex molecules, enhancing their biological activity or functional properties. Additionally, it is employed in the development of heterocyclic compounds, which are crucial in drug discovery and material science. Its versatility also extends to the synthesis of organic electronic materials, where thiazole derivatives play a role in improving performance.

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