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Structure of 147208-69-3
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(R)-2-((3aS,4S,6S,7aR)-3a,5,5-Trimethylhexahydro-4,6-methanobenzo[d][1,3,2]dioxaborol-2-yl)pyrrolidine hydrochloride features a chiral boronate moiety integrated into a rigid, bench-stable heterocyclic framework. This configuration enhances stereoselective coupling efficiency in cross-coupling reactions. The hydrochloride salt improves solubility and handling under standard conditions.
(R)-2-((3aS,4S,6S,7aR)-3a,5,5-Trimethylhexahydro-4,6-methanobenzo[d][1,3,2]dioxaborol-2-yl)pyrrolidine hydrochloride serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. Its chiral pyrrolidine core and sterically shielded boronate ester enable selective functionalization in complex molecule synthesis, with excellent functional group tolerance and compatibility in late-stage diversification workflows.
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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-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: