Rel-(3R,4R)-4-Fluoropyrrolidin-3-Amine Dihydrochloride

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Reagent Code: #231517
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CAS Number 125197-40-2

science Other reagents with same CAS 125197-40-2

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Weight 177.05 g/mol
Formula C₄H₁₁Cl₂FN₂
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of enzyme inhibitors and central nervous system agents. Its fluorinated pyrrolidine structure enhances metabolic stability and bioavailability in drug candidates. Commonly employed in the preparation of antiviral and antidepressant compounds due to its ability to mimic natural amino acids while providing improved pharmacokinetic properties. Also utilized in medicinal chemistry for structure-activity relationship studies where stereochemistry and fluorination play critical roles in target binding.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,810.00
inventory 250mg
10-20 days ฿4,510.00
inventory 1g
10-20 days ฿18,040.00
inventory 5g
10-20 days ฿78,430.00

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Rel-(3R,4R)-4-Fluoropyrrolidin-3-Amine Dihydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of enzyme inhibitors and central nervous system agents. Its fluorinated pyrrolidine structure enhances metabolic stability and bioavailability in drug candidates. Commonly employed in the preparation of antiviral and antidepressant compounds due to its ability to mimic natural amino acids while providing improved pharmacokinetic properties. Also utilized in medicinal chemistry for structure-activity relat

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of enzyme inhibitors and central nervous system agents. Its fluorinated pyrrolidine structure enhances metabolic stability and bioavailability in drug candidates. Commonly employed in the preparation of antiviral and antidepressant compounds due to its ability to mimic natural amino acids while providing improved pharmacokinetic properties. Also utilized in medicinal chemistry for structure-activity relationship studies where stereochemistry and fluorination play critical roles in target binding.

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