3-Cyclobutylthiophene-2-boronic acid pinacol ester

95%

Reagent Code: #90060
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CAS Number 2223040-29-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 282.20662 g/mol
Formula C₁₄H₂₃BO₃S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. 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 development of drug candidates, where precise molecular architecture is crucial. Additionally, it finds use in materials science for the synthesis of conjugated polymers and organic electronic materials, contributing to advancements in optoelectronics and sensors. Its cyclobutyl group can impart specific steric and electronic properties, making it suitable for tailored applications in chemical research and industrial processes.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days $465.85
inventory 25mg
10-20 days $1,365.98
3-Cyclobutylthiophene-2-boronic acid pinacol ester
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. 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 development of drug candidates, where precise molecular architecture is crucial. Additionally, it finds use in materials science for the synthesis of conjugated polymers and organic electronic materials, contributing to advancements in optoelectronics and sensors. Its cyclobutyl group can impart specific steric and electronic properties, making it suitable for tailored applications in chemical research and industrial processes.
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