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Structure of 2206737-78-0
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This fluorinated pyrrolidine derivative integrates a chiral methylated scaffold with a reactive hydroxyl group, enabling precise functionalization in medicinal chemistry. The (2S,4R) stereochemistry ensures high enantioselectivity in downstream transformations, while the bench-stable fluorine substituent enhances metabolic resilience. This compound serves as a key building block for CNS-targeted therapeutics and bioactive heterocycles.
((2S,4R)-4-Fluoro-1-methylpyrrolidin-2-yl)methanol serves as a versatile chiral building block in medicinal chemistry, enabling the construction of fluorinated pyrrolidine scaffolds prevalent in bioactive molecules. Its bench-stable nature and compatibility with standard coupling and functionalization protocols facilitate efficient synthesis of peptide mimetics and kinase inhibitors. The molecule’s defined stereochemistry and fluorine substitution enhance metabolic stability and membrane permeability, offering practical advantages in lead optimization 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: