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Structure of 1260150-04-6
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This tetrahydroquinoline-based boronic acid features a tert-butoxycarbonyl-protected amine and a boronate handle, enabling direct incorporation into Suzuki-Miyaura cross-coupling reactions. The electron-rich aromatic system enhances reactivity, while the Boc group provides stability during storage and handling.
[1-[(tert-Butoxy)carbonyl]-1,2,3,4-tetrahydroquinolin-6-yl]boronic acid serves as a stable, bench-ready building block for Suzuki-Miyaura cross-coupling reactions. The tetrahydroquinoline core provides a rigid, bioactive scaffold with demonstrated utility in medicinal chemistry. The Boc-protected amine ensures compatibility with diverse reaction conditions and facilitates downstream deprotection. Functional group tolerance and ease of purification support efficient access to complex heterocyclic architectures.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: