(1S,2R)-2-(4-Fluorophenyl)cyclopropanamine

97%

Reagent Code: #36236
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CAS Number 1207276-00-3

science Other reagents with same CAS 1207276-00-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.18 g/mol
Formula C₉H₁₀FN
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MDL Number MFCD28398056
inventory_2 Storage & Handling
Storage room temperature

description Product Description

(1S,2R)-2-(4-Fluorophenyl)cyclopropanamine is a compound with potential applications in medicinal chemistry and drug development. Its unique cyclopropane structure, combined with the presence of a fluorophenyl group, makes it a valuable intermediate in the synthesis of biologically active molecules. It is particularly relevant in the design of central nervous system (CNS) drugs, where its structural features may contribute to binding affinity and selectivity for specific receptors or enzymes. The compound's stereochemistry also plays a critical role in its pharmacological activity, making it a candidate for the development of enantioselective drugs. Additionally, its fluorine substituent can enhance metabolic stability and bioavailability, which are key considerations in drug optimization. Researchers may explore its use in creating novel antidepressants, anxiolytics, or other neuropharmacological agents due to its potential interaction with neurotransmitter systems.

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

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿17,100.00
inventory 100mg
10-20 days ฿9,000.00

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(1S,2R)-2-(4-Fluorophenyl)cyclopropanamine
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(1S,2R)-2-(4-Fluorophenyl)cyclopropanamine is a compound with potential applications in medicinal chemistry and drug development. Its unique cyclopropane structure, combined with the presence of a fluorophenyl group, makes it a valuable intermediate in the synthesis of biologically active molecules. It is particularly relevant in the design of central nervous system (CNS) drugs, where its structural features may contribute to binding affinity and selectivity for specific receptors or enzymes. The compound's stereochemistry also plays a critical role in its pharmacological activity, making it a candidate for the development of enantioselective drugs. Additionally, its fluorine substituent can enhance metabolic stability and bioavailability, which are key considerations in drug optimization. Researchers may explore its use in creating novel antidepressants, anxiolytics, or other neuropharmacological agents due to its potential interaction with neurotransmitter systems.
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