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Structure of 1314999-39-7
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This chiral pyrrolidine derivative features a sterically hindered, bench-stable 3-carboxylic acid group and a (3R)-configured stereocenter. It integrates readily into peptide-based scaffolds and serves as a conformationally restricted building block in medicinal chemistry applications.
(3R)-4,4-Dimethylpyrrolidine-3-carboxylic acid serves as a stereochemically defined proline analog, enabling the construction of constrained peptidomimetics and heterocyclic scaffolds in medicinal chemistry. Its stable chiral center and tertiary amine functionality facilitate robust coupling reactions, while the gem-dimethyl substitution enhances metabolic stability and conformational rigidity—key attributes for optimizing bioavailability in lead compound development.
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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: