5-(2-Methoxyphenyl)thiazole-4-boronic acid pinacol ester

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Reagent Code: #90762
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CAS Number 2223030-58-6

science Other reagents with same CAS 2223030-58-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 335.22618 g/mol
Formula C₁₆H₂₂BNO₄S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic ester functional group makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. It is often employed in the pharmaceutical industry for the synthesis of drug intermediates, where precise molecular architecture is crucial. Additionally, it finds use in materials science for developing advanced polymers and electronic materials, leveraging its ability to introduce thiazole and methoxyphenyl moieties into target structures. Its stability and reactivity under mild conditions make it a preferred choice for chemists working on fine chemical synthesis.

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

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5-(2-Methoxyphenyl)thiazole-4-boronic acid pinacol ester
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic ester functional group makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. It is often employed in the pharmaceutical industry for the synthesis of drug intermediates, where precise molecular architecture is crucial. Additionally, it finds use in materials science for developing advanced polymers and electronic materials, leveraging its ability to introduce thiazole and methoxyphenyl moieties into target structures. Its stability and reactivity under mild conditions make it a preferred choice for chemists working on fine chemical synthesis.
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