tert-Butyl 3-(4-chlorophenyl)piperazine-1-carboxylate

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Reagent Code: #146415
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CAS Number 886767-49-3

science Other reagents with same CAS 886767-49-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.79 g/mol
Formula C₁₅H₂₁ClN₂O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents. It serves as a building block for creating bioactive molecules due to its piperazine core, which is commonly found in drugs targeting neurological and psychiatric disorders. The tert-butyloxycarbonyl (Boc) group allows for selective protection during multi-step syntheses, enabling controlled modification of the piperazine ring. Its chlorophenyl substituent contributes to lipophilicity and receptor binding affinity, making it valuable in medicinal chemistry for optimizing drug candidates.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,740.00
inventory 5g
10-20 days ฿34,590.00
inventory 1g
10-20 days ฿6,930.00

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tert-Butyl 3-(4-chlorophenyl)piperazine-1-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents. It serves as a building block for creating bioactive molecules due to its piperazine core, which is commonly found in drugs targeting neurological and psychiatric disorders. The tert-butyloxycarbonyl (Boc) group allows for selective protection during multi-step syntheses, enabling controlled modification of the piperazine ring. Its chlorophenyl substituent contribu

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents. It serves as a building block for creating bioactive molecules due to its piperazine core, which is commonly found in drugs targeting neurological and psychiatric disorders. The tert-butyloxycarbonyl (Boc) group allows for selective protection during multi-step syntheses, enabling controlled modification of the piperazine ring. Its chlorophenyl substituent contributes to lipophilicity and receptor binding affinity, making it valuable in medicinal chemistry for optimizing drug candidates.

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