1-(4-BroMobenzyl)piperazine

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Reagent Code: #39437
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CAS Number 91345-62-9

science Other reagents with same CAS 91345-62-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.15 g/mol
Formula C₁₁H₁₅BrN₂
badge Registry Numbers
MDL Number MFCD02177416
thermostat Physical Properties
Melting Point 56-62℃(lit.)
Boiling Point 112-116℃0.3 mm Hg(lit.)
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Primarily used in pharmaceutical research, 1-(4-Bromobenzyl)piperazine serves as a key intermediate in the synthesis of various bioactive compounds. It is often employed in the development of drugs targeting neurological disorders, including antidepressants and antipsychotics, due to its structural compatibility with serotonin and dopamine receptors. Additionally, it finds application in the creation of ligands for receptor binding studies, aiding in the exploration of new therapeutic pathways. Its bromine moiety also makes it a valuable building block in organic synthesis, particularly in cross-coupling reactions to form more complex molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,485.00
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1-(4-BroMobenzyl)piperazine
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Primarily used in pharmaceutical research, 1-(4-Bromobenzyl)piperazine serves as a key intermediate in the synthesis of various bioactive compounds. It is often employed in the development of drugs targeting neurological disorders, including antidepressants and antipsychotics, due to its structural compatibility with serotonin and dopamine receptors. Additionally, it finds application in the creation of ligands for receptor binding studies, aiding in the exploration of new therapeutic pathways. Its bromi

Primarily used in pharmaceutical research, 1-(4-Bromobenzyl)piperazine serves as a key intermediate in the synthesis of various bioactive compounds. It is often employed in the development of drugs targeting neurological disorders, including antidepressants and antipsychotics, due to its structural compatibility with serotonin and dopamine receptors. Additionally, it finds application in the creation of ligands for receptor binding studies, aiding in the exploration of new therapeutic pathways. Its bromine moiety also makes it a valuable building block in organic synthesis, particularly in cross-coupling reactions to form more complex molecules.

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