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Structure of 66217-55-8
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2-Cyclopentyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a bench-stable boronate reagent featuring a cyclopentyl group that enhances lipophilicity and metabolic stability. The tetramethyl substitution pattern confers exceptional air and moisture tolerance, enabling reliable use in Suzuki-Miyaura cross-coupling reactions under standard conditions. This derivative integrates seamlessly into complex molecular architectures with minimal side-reaction risk.
2-Cyclopentyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boron reagent for Suzuki-Miyaura cross-coupling reactions. Its sterically protected boronate moiety enables high functional group tolerance and reliable coupling with aryl and vinyl halides. The cyclopentyl substituent provides enhanced solubility and compatibility in polar reaction media, facilitating efficient transformations in medicinal chemistry and process-scale 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-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: