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Structure of 96293-17-3
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This chiral scaffold integrates a benzylproline-derived amine with a benzophenone core, enabling asymmetric synthesis of bioactive compounds. The stereogenic center at the proline moiety ensures high enantioselectivity in catalytic transformations, while the aromatic ketone serves as a robust handle for further functionalization under standard conditions.
(S)-2-(N-Benzylprolyl)aminobenzophenone serves as a chiral building block for synthesizing bioactive heterocycles and peptidomimetics. Its amine functionality enables straightforward derivatization, while the benzophenone core offers structural rigidity and π-stacking potential. The molecule exhibits bench stability and compatibility with standard coupling conditions, facilitating incorporation into complex scaffolds via amide bond formation or reductive amination.
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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: