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Structure of 160032-40-6
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Thieno[3,2-b]thiophen-2-ylboronic acid features a fused thiophene core that enhances electronic delocalization and stability. This boronate moiety integrates readily into Suzuki-Miyaura cross-coupling reactions under standard conditions, enabling efficient access to conjugated heteroaryl architectures. The compound exhibits bench-stable handling and moisture-tolerant reactivity, simplifying synthetic workflows in materials and pharmaceutical development.
Thieno[3,2-b]thiophen-2-ylboronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl architectures. Its boronic acid functionality exhibits good bench stability and tolerates a range of functional groups, facilitating direct incorporation into complex molecular frameworks. This compound functions effectively in the synthesis of advanced heterocyclic systems and conjugated materials, offering reliable reactivity under standard coupling conditions.
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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 : H315-H319
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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: