(2-(4-Fluorophenyl)cyclopropyl)methanamine hydrochloride

98%

Reagent Code: #188861
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CAS Number 1354954-53-2

science Other reagents with same CAS 1354954-53-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.67 g/mol
Formula C₁₀H₁₃ClFN
badge Registry Numbers
MDL Number MFCD20502100
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) active compounds. Its structural motif is valuable in creating analogs for serotonin and dopamine receptor modulators. The compound is also employed in the preparation of selective inhibitors for enzymes involved in neurological pathways, making it relevant in research for antidepressants and anxiolytic drugs. Due to the presence of the amine functionality and the strained cyclopropane ring, it serves as a building block in medicinal chemistry for structure-activity relationship (SAR) studies. Its fluorinated aryl group enhances binding affinity and metabolic stability in resulting drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,430.00
inventory 1g
10-20 days ฿34,960.00
inventory 250mg
10-20 days ฿11,880.00

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(2-(4-Fluorophenyl)cyclopropyl)methanamine hydrochloride
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Used primarily as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) active compounds. Its structural motif is valuable in creating analogs for serotonin and dopamine receptor modulators. The compound is also employed in the preparation of selective inhibitors for enzymes involved in neurological pathways, making it relevant in research for antidepressants and anxiolytic drugs. Due to the presence of the amine functionality and the strained cyclopropane ring, it serves as a building block in medicinal chemistry for structure-activity relationship (SAR) studies. Its fluorinated aryl group enhances binding affinity and metabolic stability in resulting drug candidates.
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