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*For research and further manufacturing use only, not for direct human use.
Structure of 1232132-73-8
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This boronate reagent features a sterically hindered dioxaborolane ring paired with a 2,3-dimethylphenyl group, enhancing stability and resistance to protodeboronation. The electron-rich aryl moiety enables efficient coupling in Suzuki-Miyaura reactions under mild conditions, delivering high yields with minimal byproduct formation.
2-(2,3-Dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. Its ortho-dimethyl substitution enhances electronic modulation and steric profile, enabling efficient coupling with aryl halides and triflates under mild conditions. The tetramethyl-substituted dioxaborolane ring ensures excellent shelf stability, minimal protodeboronation, and straightforward purification, making it ideal for iterative synthesis of complex biaryl 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-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: