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Structure of 130798-48-0
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(R)-Di(naphthalen-2-yl)(pyrrolidin-2-yl)methanol features a chiral benzylic center flanked by two naphthyl groups and a pyrrolidine moiety, delivering high stereochemical integrity. This sterically encumbered scaffold enables selective coupling in asymmetric synthesis, particularly in transition-metal-catalyzed cross-coupling reactions. The molecule exhibits robust stability under standard bench conditions and facilitates efficient ligand integration in catalytic systems requiring rigid, electron-rich coordination environments.
(R)-Di(naphthalen-2-yl)(pyrrolidin-2-yl)methanol serves as a chiral, bench-stable building block for asymmetric synthesis, enabling the construction of complex heterocyclic scaffolds through stereoselective transformations. Its three distinct aromatic and nitrogen-containing moieties offer orthogonal reactivity, facilitating functionalization in multi-step sequences. The molecule functions effectively in catalytic systems requiring defined stereochemistry and exhibits favorable solubility and purification characteristics in standard organic 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: