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Structure of 1268683-45-9
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This boronate moiety integrates a hydroxymethyl-functionalized thiophene scaffold, enabling efficient cross-coupling under standard conditions. The pendant hydroxyl group enhances solubility and facilitates downstream derivatization, while the boronic acid functionality ensures compatibility with Suzuki-Miyaura reactions.
(5-(Hydroxymethyl)thiophen-3-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl architectures. The boronic acid moiety exhibits good bench stability and tolerates a range of functional groups, facilitating straightforward purification and integration into complex molecular scaffolds common in 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: