1-Benzyl 2-methyl (S)-piperazine-1,2-dicarboxylate

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Reagent Code: #141393
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CAS Number 314741-63-4

science Other reagents with same CAS 314741-63-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.3 g/mol
Formula C₁₄H₁₈N₂O₄
badge Registry Numbers
MDL Number MFCD04115342
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules and chiral drugs. Its structure supports the construction of complex piperazine-based frameworks common in central nervous system agents, enzyme inhibitors, and receptor antagonists. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the presence of functional handles for further derivatization. Also utilized in asymmetric synthesis where the chiral center aids in stereoselective transformations.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,280.00
inventory 1g
10-20 days ฿14,220.00
inventory 5g
10-20 days ฿49,740.00

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1-Benzyl 2-methyl (S)-piperazine-1,2-dicarboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules and chiral drugs. Its structure supports the construction of complex piperazine-based frameworks common in central nervous system agents, enzyme inhibitors, and receptor antagonists. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the presence of functional handles for further derivatization. Also utilized in asymmetric synthesis wh

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules and chiral drugs. Its structure supports the construction of complex piperazine-based frameworks common in central nervous system agents, enzyme inhibitors, and receptor antagonists. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the presence of functional handles for further derivatization. Also utilized in asymmetric synthesis where the chiral center aids in stereoselective transformations.

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