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Structure of 206551-43-1
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5-Acetylthiophene-2-boronic acid features a thiophene scaffold with complementary boronic acid and acetyl functionalities, enabling direct incorporation into Suzuki-Miyaura coupling reactions. The electron-deficient thiophene ring enhances reactivity, while the boronic acid group offers stability under standard conditions. This bifunctional architecture supports efficient synthesis of complex heterocyclic architectures in medicinal chemistry and materials science.
5-Acetylthiophene-2-boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl architectures. The acetyl group provides orthogonal reactivity for downstream functionalization, while the boronic acid moiety ensures compatibility with aqueous conditions and broad functional group tolerance. Bench-stable and readily purified by recrystallization, it facilitates scalable synthesis of complex scaffolds relevant to medicinal chemistry and materials science.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: