1-((3-Bromo-4-ethoxyphenyl)sulfonyl)-4-methylpiperazine

≥95%

Reagent Code: #114260
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CAS Number 1093065-11-2

science Other reagents with same CAS 1093065-11-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 363.27 g/mol
Formula C₁₃H₁₉BrN₂O₃S
badge Registry Numbers
MDL Number MFCD27923092
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in pharmaceutical research and development due to its structural properties, which make it a potential candidate for drug discovery. It is often explored for its biological activity, particularly in targeting specific enzymes or receptors involved in disease pathways. Researchers investigate its efficacy in treating conditions such as neurological disorders, inflammation, or cancer, depending on its interaction with biological systems. Additionally, it may serve as an intermediate in the synthesis of more complex molecules, contributing to the development of novel therapeutic agents. Its sulfonyl and piperazine groups are key functional moieties that enhance its binding affinity and selectivity in drug design.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,069.00
inventory 250mg
10-20 days ฿6,147.00

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1-((3-Bromo-4-ethoxyphenyl)sulfonyl)-4-methylpiperazine
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This compound is primarily utilized in pharmaceutical research and development due to its structural properties, which make it a potential candidate for drug discovery. It is often explored for its biological activity, particularly in targeting specific enzymes or receptors involved in disease pathways. Researchers investigate its efficacy in treating conditions such as neurological disorders, inflammation, or cancer, depending on its interaction with biological systems. Additionally, it may serve as an intermediate in the synthesis of more complex molecules, contributing to the development of novel therapeutic agents. Its sulfonyl and piperazine groups are key functional moieties that enhance its binding affinity and selectivity in drug design.
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