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Structure of 1191062-02-8
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This boronate moiety integrates a tert-butyl carbamate-protected piperidine ring, enabling stable coupling in Suzuki-Miyaura reactions. The electron-deficient arylboronic acid features enhanced solubility and moisture tolerance, simplifying handling in synthetic workflows.
4-(1-(tert-Butoxycarbonyl)piperidin-4-yl)phenylboronic acid serves as a versatile building block for Suzuki-Miyaura coupling reactions, enabling efficient construction of biaryl scaffolds in medicinal chemistry and materials science. The piperidine moiety is protected as a stable tert-butyl carbamate, offering excellent bench stability and compatibility with diverse reaction conditions. Its boronic acid functionality facilitates reliable cross-coupling under mild, palladium-catalyzed protocols, making it ideal for late-stage functionalization and modular synthesis of 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: