(S)-tert-Butyl 3-ethylpiperazine-1-carboxylate

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Reagent Code: #234924
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CAS Number 928025-56-3

science Other reagents with same CAS 928025-56-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.31 g/mol
Formula C₁₁H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD07772110
thermostat Physical Properties
Boiling Point 287°C
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 active pharmaceutical ingredients (APIs) that require chiral piperazine scaffolds. Its protected amine group allows for selective reactions in multi-step organic syntheses, making it valuable in drug discovery for central nervous system agents, antipsychotics, and other bioactive molecules. The tert-butyl carbamate (Boc) protection ensures stability during reactions and can be easily removed under mild acidic conditions when needed. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical purity and structural versatility.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿468.00
inventory 1g
10-20 days ฿2,620.00
inventory 5g
10-20 days ฿12,000.00

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(S)-tert-Butyl 3-ethylpiperazine-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 chiral piperazine scaffolds. Its protected amine group allows for selective reactions in multi-step organic syntheses, making it valuable in drug discovery for central nervous system agents, antipsychotics, and other bioactive molecules. The tert-butyl carbamate (Boc) protection ensures stability during reactions and can be easily removed under mil

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that require chiral piperazine scaffolds. Its protected amine group allows for selective reactions in multi-step organic syntheses, making it valuable in drug discovery for central nervous system agents, antipsychotics, and other bioactive molecules. The tert-butyl carbamate (Boc) protection ensures stability during reactions and can be easily removed under mild acidic conditions when needed. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical purity and structural versatility.

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