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Structure of 61350-65-0
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(R)-2-(Pyrrolidin-2-yl)acetic acid features a chiral pyrrolidine ring tethered to a carboxylic acid moiety, delivering a rigid, electron-rich scaffold ideal for asymmetric synthesis. This bench-stable derivative integrates readily into peptidomimetics and bioactive molecule frameworks, offering enhanced solubility and conformational control in medicinal chemistry applications.
(R)-2-(Pyrrolidin-2-yl)acetic acid serves as a versatile chiral building block in medicinal chemistry, enabling the synthesis of bioactive molecules through standard amide coupling and functional group manipulation. Its pyrrolidine moiety provides favorable solubility and metabolic stability, while the α–amino acid framework supports direct incorporation into peptide-like scaffolds. Bench-stable and readily purified by recrystallization, it functions reliably in both small-molecule and macrocyclic synthesis 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: