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Structure of 1257651-17-4
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Tert-butyl (2-oxo-2-((3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)amino)ethyl)carbamate is a bench-stable boronate ester bearing a para-aminoaryl handle, enabling direct coupling in Suzuki-Miyaura reactions. This carbamate-protected scaffold integrates seamlessly into peptide and heterocyclic scaffolds under standard conditions, delivering high functional group tolerance and minimal decomposition during purification workflows.
Tert-butyl (2-oxo-2-((3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)amino)ethyl)carbamate serves as a stable, bench-ready boron-containing building block for Suzuki-Miyaura cross-coupling reactions. The dioxaborolane moiety enables efficient coupling with aryl and heteroaryl halides under mild conditions, while the tert-butyl carbamate group provides orthogonal protection for primary amines. Its functional group tolerance and compatibility with standard reaction protocols make it ideal for constructing complex scaffolds in medicinal chemistry and materials science applications.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: