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Structure of 1150114-78-5
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This boronic acid features a chloro-substituted aromatic ring with a formyl group positioned ortho to the boronate moiety. The electrophilic formyl function enables direct coupling in Suzuki-Miyaura reactions, while the chlorine atom serves as a latent handle for downstream functionalization. Bench-stable and moisture-tolerant, it streamlines access to complex heterocycles and bioactive scaffolds in medicinal chemistry workflows.
(2-Chloro-5-formylphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling the efficient construction of biaryl scaffolds under mild conditions. The formyl group provides orthogonal reactivity for downstream functionalization via oxime or hydrazone formation, while the boronic acid moiety offers excellent bench stability and compatibility with diverse reaction partners. Its dual functionality facilitates rapid access to complex molecular architectures 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: