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Structure of 917985-54-7
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This boronate ester features a hexylthiophene moiety enabling efficient coupling in Suzuki-Miyaura reactions. The tetramethyl-1,3,2-dioxaborolane scaffold imparts stability and ease of handling, while the alkylthiophene group enhances solubility and electronic tuning for conjugated polymer synthesis.
2-(5-Hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. The hexylthiophene moiety provides enhanced solubility and facilitates access to conjugated π-systems, while the tetramethyl-substituted dioxaborolane offers excellent air and moisture stability. It enables efficient construction of functionalized thiophene-based scaffolds in organic synthesis and materials chemistry with high yield and minimal purification challenges.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: