(S)-3-Fluoropyrrolidine hydrochloride

97%

Reagent Code: #113781
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CAS Number 136725-53-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 125.57 g/mol
Formula C₄H₉ClFN
thermostat Physical Properties
Melting Point 183-187°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

(S)-3-Fluoropyrrolidine hydrochloride is widely utilized in pharmaceutical research and development, particularly in the synthesis of bioactive molecules and drug candidates. Its unique structure, featuring a fluorinated pyrrolidine ring, makes it a valuable building block for designing compounds with enhanced metabolic stability and binding affinity. It is often employed in the creation of small molecule inhibitors, receptor agonists, and antagonists, targeting various diseases such as neurological disorders and cancer. Additionally, its chiral nature allows for the development of enantiomerically pure drugs, improving therapeutic efficacy and reducing side effects. The compound is also used in medicinal chemistry to explore structure-activity relationships (SAR) and optimize drug-like properties.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White Solid
Purity (%) 96.5-100%
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days £171.93
inventory 250mg
10-20 days £14.94
inventory 1g
10-20 days £43.90
(S)-3-Fluoropyrrolidine hydrochloride
(S)-3-Fluoropyrrolidine hydrochloride is widely utilized in pharmaceutical research and development, particularly in the synthesis of bioactive molecules and drug candidates. Its unique structure, featuring a fluorinated pyrrolidine ring, makes it a valuable building block for designing compounds with enhanced metabolic stability and binding affinity. It is often employed in the creation of small molecule inhibitors, receptor agonists, and antagonists, targeting various diseases such as neurological disorders and cancer. Additionally, its chiral nature allows for the development of enantiomerically pure drugs, improving therapeutic efficacy and reducing side effects. The compound is also used in medicinal chemistry to explore structure-activity relationships (SAR) and optimize drug-like properties.
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