Thiophene-2-boronic acid pinacol ester
97%
Reagent
Code: #91130
Alias
Thiophene-2-boronic acid pinacol ester 2-thiophene boric acid pinacol ester
CAS Number
193978-23-3
blur_circular Chemical Specifications
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Molecular Information
Weight
210.1 g/mol
Formula
C₁₀H₁₅BO₂S
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Registry Numbers
MDL Number
MFCD05663878
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Physical Properties
Melting Point
68-70°C
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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.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Purity (GC) | 96.5-100% |
Sulfur | 14.5-16 |
Appearance | White to beige powder or crystals |
Infrared Spectrum | Conforms to Structure |
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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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