5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thieno[2,3-b]pyridine
≥95%
Reagent
Code: #241712
CAS Number
1034579-02-6
blur_circular Chemical Specifications
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Molecular Information
Weight
261.15 g/mol
Formula
C₁₃H₁₆BNO₂S
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Registry Numbers
MDL Number
MFCD12923404
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Storage & Handling
Storage
2-8°C, stored in inert gas
description Product Description
Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of pharmaceuticals and organic electronic materials. Its boron-containing group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-carbon bonds in drug discovery and development. It is especially valuable in constructing thienopyridine-based scaffolds, which are common in bioactive molecules and kinase inhibitors. Additionally, it finds use in materials science for building conjugated systems in organic semiconductors and optoelectronic devices.
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