2-(4-hexylphenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
98%
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Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl or vinyl halides, making it valuable in the preparation of conjugated organic materials. Commonly employed in the synthesis of liquid crystals, organic semiconductors, and pharmaceuticals where a hexyl-substituted phenyl moiety is required. The hexyl chain enhances solubility in organic solvents, improving reaction efficiency in homogeneous conditions. Also utilized in the development of advanced materials for optoelectronic devices such as OLEDs and OFETs due to its ability to tune molecular packing and electronic properties.
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