5-(3-Fluorophenyl)thiophene-2-boronic acid pinacol ester

95%

Reagent Code: #90777
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CAS Number 1402174-30-4

science Other reagents with same CAS 1402174-30-4

blur_circular Chemical Specifications

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Weight 322.2026032 g/mol
Formula C₁₆H₂₀BFO₃S
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 like the Suzuki-Miyaura reaction. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical and materials science industries. The boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. Its fluorophenyl moiety can enhance the biological activity or modify the electronic properties of the resulting compounds, making it valuable in drug development and the design of functional materials. Additionally, its stability and reactivity make it a preferred choice for synthesizing intermediates in the production of agrochemicals and organic electronic materials.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿8,982.00
inventory 25mg
10-20 days ฿19,800.00

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5-(3-Fluorophenyl)thiophene-2-boronic acid pinacol ester
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical and materials science industries. The boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. Its fluorophenyl moiety can enhance the biological activity or modify the electronic properties of the re

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical and materials science industries. The boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. Its fluorophenyl moiety can enhance the biological activity or modify the electronic properties of the resulting compounds, making it valuable in drug development and the design of functional materials. Additionally, its stability and reactivity make it a preferred choice for synthesizing intermediates in the production of agrochemicals and organic electronic materials.

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