2-(5-Chlorothiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
96%
Reagent
Code: #160292
CAS Number
635305-24-7
blur_circular Chemical Specifications
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Molecular Information
Weight
244.55 g/mol
Formula
C₁₀H₁₄BClO₂S
thermostat
Physical Properties
Boiling Point
360.9°C
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Storage & Handling
Storage
2-8°C
description Product Description
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl or vinyl halides under mild conditions, making it valuable for constructing complex organic molecules. Commonly employed in the development of conjugated materials for electronics and in late-stage functionalization of bioactive compounds due to its stability and reactivity profile.
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