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Structure of 2246849-87-4
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This boronate reagent features a tert-butoxycarbonyl-protected amine and a chlorine substituent on the phenyl ring, enabling selective coupling in late-stage functionalization. The electron-deficient arylboronic acid unit delivers enhanced reactivity in Suzuki-Miyaura cross-coupling, while the Boc group ensures stability during storage and handling under standard conditions.
(5-((Tert-butoxycarbonyl)amino)-2-chlorophenyl)boronic acid serves as a versatile building block for the synthesis of bioactive heterocycles and pharmaceutical intermediates. The boronic acid functionality enables palladium-catalyzed cross-coupling reactions, while the ortho-chloro group permits subsequent nucleophilic substitution or cyclization. The tert-butoxycarbonyl (Boc) protecting group offers excellent bench stability and compatibility with standard deprotection protocols, facilitating efficient multi-step synthesis.
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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: