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Structure of 330794-35-9
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This boronate ester features a tert-butyl carbamate-protected amine tethered to a para-substituted benzyl group, enabling stable coupling in Suzuki-Miyaura reactions. The tetramethyl-dioxaborolane moiety delivers high functional group tolerance and compatibility with diverse reaction conditions. Designed for efficient incorporation into complex molecular architectures, this reagent streamlines access to biaryl and arylalkyl scaffolds in medicinal chemistry and materials synthesis.
tert-Butyl (4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)carbamate serves as a versatile boron-containing building block for Suzuki-Miyaura cross-coupling reactions. The boryl group enables efficient C–C bond formation under mild conditions, while the tert-butyl carbamate protects the primary amine and enhances stability during storage and handling. Its compatibility with diverse functional groups and ease of purification make it ideal for constructing complex aromatic scaffolds in medicinal chemistry and process development workflows.
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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: