2-((4-Chlorophenyl)(piperidin-4-yloxy)methyl)pyridine 4-nitrobenzoate

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Reagent Code: #46727
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CAS Number 161558-45-8

science Other reagents with same CAS 161558-45-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 469.92 g/mol
Formula C₂₄H₂₄ClN₃O₅
badge Registry Numbers
MDL Number MFCD19105231
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a potential bioactive molecule. It is studied for its role in the development of new pharmaceutical agents, particularly in the design of drugs targeting the central nervous system. The structure suggests potential interactions with receptors or enzymes in the brain, making it a candidate for researching treatments for neurological disorders such as anxiety, depression, or neurodegenerative diseases. Additionally, its nitrobenzoate moiety may contribute to its use in prodrug formulations, where it could enhance bioavailability or stability. Research is ongoing to explore its efficacy, safety, and specific mechanisms of action in various therapeutic applications.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Pale red solid
Purity 98.5-100
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿940.00
inventory 25g
10-20 days ฿11,600.00
inventory 5g
10-20 days ฿3,300.00
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2-((4-Chlorophenyl)(piperidin-4-yloxy)methyl)pyridine 4-nitrobenzoate
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This compound is primarily utilized in the field of medicinal chemistry as a potential bioactive molecule. It is studied for its role in the development of new pharmaceutical agents, particularly in the design of drugs targeting the central nervous system. The structure suggests potential interactions with receptors or enzymes in the brain, making it a candidate for researching treatments for neurological disorders such as anxiety, depression, or neurodegenerative diseases. Additionally, its nitrobenzoate moiety may contribute to its use in prodrug formulations, where it could enhance bioavailability or stability. Research is ongoing to explore its efficacy, safety, and specific mechanisms of action in various therapeutic applications.
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