tert-butyl 4-[2-(4-nitrophenyl)acetyl]piperazine-1-carboxylate

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Reagent Code: #242786
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CAS Number 643087-38-1

science Other reagents with same CAS 643087-38-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 349.38 g/mol
Formula C₁₇H₂₃N₃O₅
badge Registry Numbers
MDL Number MFCD31803577
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that require piperazine-based structures. Its nitrophenyl acetyl group enables further chemical modifications, making it valuable in constructing drug candidates for central nervous system agents, antipsychotics, or antimicrobial compounds. Commonly employed in research laboratories for building complex molecules through reduction, coupling, or deprotection reactions. The tert-butyl carbamate (Boc) protection allows for controlled deprotection under mild acidic conditions, facilitating stepwise synthesis in multi-step organic reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,410.00
inventory 250mg
10-20 days ฿3,670.00

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tert-butyl 4-[2-(4-nitrophenyl)acetyl]piperazine-1-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that require piperazine-based structures. Its nitrophenyl acetyl group enables further chemical modifications, making it valuable in constructing drug candidates for central nervous system agents, antipsychotics, or antimicrobial compounds. Commonly employed in research laboratories for building complex molecules through reduction, coupling, or deprotection rea

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that require piperazine-based structures. Its nitrophenyl acetyl group enables further chemical modifications, making it valuable in constructing drug candidates for central nervous system agents, antipsychotics, or antimicrobial compounds. Commonly employed in research laboratories for building complex molecules through reduction, coupling, or deprotection reactions. The tert-butyl carbamate (Boc) protection allows for controlled deprotection under mild acidic conditions, facilitating stepwise synthesis in multi-step organic reactions.

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