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Structure of 7076-23-5
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(R)-3-(Pyrrolidin-2-yl)pyridine features a chiral pyrrolidine ring attached to the pyridine core, delivering enhanced solubility and tunable basicity. This configuration enables precise coordination in asymmetric catalysis and facilitates integration into bioactive scaffolds. The compound exhibits bench-stable handling under standard conditions and serves as a key building block in medicinal chemistry.
(R)-3-(Pyrrolidin-2-yl)pyridine serves as a versatile chiral building block in medicinal chemistry, enabling the construction of bioactive heterocycles through standard coupling and functionalization protocols. Its pyridyl nitrogen and secondary amine functionality offer orthogonal reactivity for metal-catalyzed transformations and derivatization. The compound exhibits bench stability and facilitates purification via standard chromatographic methods, making it well-suited for iterative synthesis campaigns in API 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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: