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Structure of 1596339-08-0
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This boronate moiety integrates readily into Suzuki-Miyaura cross-coupling reactions under standard conditions. The methoxycarbonyl group enhances solubility and stability, while the thiophene scaffold provides a rigid, electron-deficient platform for efficient functionalization in synthetic organic chemistry and materials science applications.
[2-(Methoxycarbonyl)thiophen-3-yl]boronic acid serves as a versatile building block for Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds. Its thiophene core provides structural rigidity and electronic modulation, while the boronic acid and ester functionalities offer orthogonal reactivity for downstream transformations. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis in medicinal chemistry and materials science applications.
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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: