(2-Amino-4-bromophenyl) [4-(methylsulfonyl) - 1-piperazinyl] ketone

95%

Reagent Code: #36366
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CAS Number 1539817-33-8

science Other reagents with same CAS 1539817-33-8

blur_circular Chemical Specifications

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Weight 362.24274 g/mol
Formula C₁₂H₁₆BrN₃O₃S
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

(2-Amino-4-bromophenyl) [4-(methylsulfonyl)-1-piperazinyl] ketone is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel compounds with potential therapeutic applications. Its structure, featuring both a bromophenyl group and a piperazinyl moiety, makes it a valuable intermediate in the design of molecules targeting central nervous system disorders. Researchers often explore its use in creating ligands for receptors involved in neurological pathways, such as dopamine or serotonin receptors, due to its ability to modulate receptor activity. Additionally, its sulfonyl group enhances its potential as a precursor in the development of anti-inflammatory or anticancer agents, as sulfonamides are known for their biological activity. The compound's versatility also extends to organic synthesis, where it serves as a building block for more complex chemical structures in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿11,592.00
inventory 1g
10-20 days ฿27,792.00
inventory 5g
10-20 days ฿72,792.00

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(2-Amino-4-bromophenyl) [4-(methylsulfonyl) - 1-piperazinyl] ketone
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(2-Amino-4-bromophenyl) [4-(methylsulfonyl)-1-piperazinyl] ketone is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel compounds with potential therapeutic applications. Its structure, featuring both a bromophenyl group and a piperazinyl moiety, makes it a valuable intermediate in the design of molecules targeting central nervous system disorders. Researchers often explore its use in creating ligands for receptors involved in neurological pathways, such as dopamine or serotonin receptors, due to its ability to modulate receptor activity. Additionally, its sulfonyl group enhances its potential as a precursor in the development of anti-inflammatory or anticancer agents, as sulfonamides are known for their biological activity. The compound's versatility also extends to organic synthesis, where it serves as a building block for more complex chemical structures in medicinal chemistry.
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