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Structure of 1004784-50-2
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This boronate ester integrates a thieno[3,2-b]thiophene unit with high thermal stability and enhanced solubility in organic solvents. The tetramethyl-substituted dioxaborolane ring ensures excellent shelf life and resistance to hydrolysis under standard conditions. It enables efficient Suzuki-Miyaura couplings with minimal protodeboronation, delivering precise C–C bond formation in complex heterocyclic systems.
4,4,5,5-Tetramethyl-2-(thieno[3,2-b]thiophen-2-yl)-1,3,2-dioxaborolane serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. The thieno[3,2-b]thiophene moiety imparts enhanced electronic properties and metabolic stability, making it particularly useful in the synthesis of conjugated materials and functionalized heterocycles. Its high functional group tolerance and ease of purification enable reliable integration into complex molecular architectures.
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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-P405-P501
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Lot numbers can be found on the outside label of a product: