Thiophene-3-boronic acid, pinacol ester

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Reagent Code: #91131
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CAS Number 214360-70-0

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.1 g/mol
Formula C₁₀H₁₅BO₂S
badge Registry Numbers
MDL Number MFCD05663893
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Thiophene-3-boronic acid, pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This compound serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical industry, where it aids in the development of drugs and bioactive compounds. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable for synthesizing thiophene derivatives, which are essential in materials science for creating conductive polymers and organic semiconductors. Additionally, it is utilized in the production of agrochemicals and advanced materials due to its stability and reactivity in various chemical transformations.

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Test Parameter Specification
Appearance White to off-white solid
Purity 95.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,410.00
inventory 5g
10-20 days ฿5,540.00

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Thiophene-3-boronic acid, pinacol ester
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Thiophene-3-boronic acid, pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This compound serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical industry, where it aids in the development of drugs and bioactive compounds. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable for synthesizing thiophene derivatives, which are essential in materials science for creating

Thiophene-3-boronic acid, pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This compound serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical industry, where it aids in the development of drugs and bioactive compounds. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable for synthesizing thiophene derivatives, which are essential in materials science for creating conductive polymers and organic semiconductors. Additionally, it is utilized in the production of agrochemicals and advanced materials due to its stability and reactivity in various chemical transformations.

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