1-(2-Fluorobenzyl)piperazine

96%

Reagent Code: #86497
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CAS Number 89292-78-4

science Other reagents with same CAS 89292-78-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.25 g/mol
Formula C₁₁H₁₅FN₂
badge Registry Numbers
MDL Number MFCD02256027
thermostat Physical Properties
Boiling Point 93 - 96 ℃ at 0.3 百帕 - lit.
inventory_2 Storage & Handling
Density 1.170 g/mL at 25 ℃(lit.)
Storage room temperature

description Product Description

Primarily utilized in the field of medicinal chemistry, this compound serves as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure is particularly valuable in the development of compounds targeting the central nervous system, where it can be incorporated into drugs designed to interact with neurotransmitter receptors. Additionally, it has been explored in the creation of potential therapeutic agents for psychiatric and neurological disorders, such as anxiety and depression, due to its ability to modulate receptor activity. The fluorobenzyl group enhances the binding affinity and metabolic stability of the resulting compounds, making it a crucial component in drug discovery and development processes.

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Test Parameter Specification
Appearance Colorless to Tan Liquid
Purity 95.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿5,870.00
inventory 1g
10-20 days ฿1,750.00

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1-(2-Fluorobenzyl)piperazine
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Primarily utilized in the field of medicinal chemistry, this compound serves as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure is particularly valuable in the development of compounds targeting the central nervous system, where it can be incorporated into drugs designed to interact with neurotransmitter receptors. Additionally, it has been explored in the creation of potential therapeutic agents for psychiatric and neurological disorders, such as anxiety and depression, due to its ability to modulate receptor activity. The fluorobenzyl group enhances the binding affinity and metabolic stability of the resulting compounds, making it a crucial component in drug discovery and development processes.
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