Thiophene-2-boronic acid pinacol ester

97%

Reagent Code: #91130
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Alias Thiophene-2-boronic acid pinacol ester 2-thiophene boric acid pinacol ester
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CAS Number 193978-23-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.1 g/mol
Formula C₁₀H₁₅BO₂S
badge Registry Numbers
MDL Number MFCD05663878
thermostat Physical Properties
Melting Point 68-70°C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Thiophene-2-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. The compound serves as a key intermediate in the synthesis of complex organic molecules, including heterocyclic compounds. Its stability and reactivity make it a preferred choice in the development of electronic materials, such as organic semiconductors and conductive polymers. Additionally, it is employed in the creation of ligands for catalysis and in the modification of polymers to enhance their properties. Its applications extend to research and development in medicinal chemistry, where it aids in the design of novel drug candidates.

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Test Parameter Specification
Purity (GC) 96.5-100%
Sulfur 14.5-16
Appearance White to beige powder or crystals
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿270.00
inventory 5g
10-20 days ฿610.00
inventory 25g
10-20 days ฿2,880.00
Thiophene-2-boronic acid pinacol ester
Thiophene-2-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. The compound serves as a key intermediate in the synthesis of complex organic molecules, including heterocyclic compounds. Its stability and reactivity make it a preferred choice in the development of electronic materials, such as organic semiconductors and conductive polymers. Additionally, it is employed in the creation of ligands for catalysis and in the modification of polymers to enhance their properties. Its applications extend to research and development in medicinal chemistry, where it aids in the design of novel drug candidates.
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