Thiophene-2-boronic acid pinacol ester

97%

  • Product Code: 91130
  Alias:    Thiophene-2-boronic acid pinacol ester 2-thiophene boric acid pinacol ester
  CAS:    193978-23-3
Molecular Weight: 210.1 g./mol Molecular Formula: C₁₀H₁₅BO₂S
EC Number: MDL Number: MFCD05663878
Melting Point: 68-70°C Boiling Point:
Density: Storage Condition: room temperature
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.
Product Specification:
Test Specification
PURITY GC 96.5 100%
SULFUR 14.5-16
APPEARANCE White to beige powder or crystals
INFRARED SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿270.00
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-
5.000 10-20 days ฿610.00
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-
25.000 10-20 days ฿2,880.00
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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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