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Structure of 96293-19-5
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Ni-(S)-BPB-GLy delivers a chiral, bench-stable ligand platform for asymmetric catalysis, featuring a rigid bicyclic scaffold that enforces stereocontrol. This nickel complex integrates a boronate ester group with a glycine-derived chiral backbone, enabling efficient cross-coupling under mild conditions. The system exhibits high enantioselectivity in C–C bond formation, particularly suited for late-stage functionalization of bioactive molecules.
Ni-(S)-BPB-GLy serves as a highly effective chiral catalyst for asymmetric hydrogenation reactions, enabling enantioselective synthesis of valuable β-amino acid derivatives and pharmaceutical intermediates. Its robust bench stability and excellent functional group tolerance facilitate straightforward purification and scalability in industrial R&D workflows. The ligand’s well-defined stereochemistry ensures high enantiomeric excess in target molecules, making it a reliable choice for constructing chiral scaffolds in medicinal chemistry applications.
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GHS Pictogram :
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GHS No : GHS07,GHS08
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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-H351-H361
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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: