(S)-1-tert-Butyl 3-methyl piperazine-1,3-dicarboxylate

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Reagent Code: #234935
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CAS Number 314741-39-4

science Other reagents with same CAS 314741-39-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.29 g/mol
Formula C₁₁H₂₀N₂O₄
thermostat Physical Properties
Boiling Point 321.3°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key chiral intermediate in the synthesis of active pharmaceutical ingredients, particularly in the development of central nervous system (CNS) drugs and antipsychotic medications. Its stereochemistry allows for selective interactions with biological targets, improving drug efficacy and reducing side effects. Commonly employed in medicinal chemistry for constructing complex piperazine-based structures due to its protected functional groups, which enable stepwise derivatization. Also utilized in the preparation of protease inhibitors and receptor agonists/antagonists in research settings.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,130.00
inventory 10g
10-20 days ฿4,180.00
inventory 25g
10-20 days ฿8,640.00
inventory 100g
10-20 days ฿32,000.00
(S)-1-tert-Butyl 3-methyl piperazine-1,3-dicarboxylate
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Used as a key chiral intermediate in the synthesis of active pharmaceutical ingredients, particularly in the development of central nervous system (CNS) drugs and antipsychotic medications. Its stereochemistry allows for selective interactions with biological targets, improving drug efficacy and reducing side effects. Commonly employed in medicinal chemistry for constructing complex piperazine-based structures due to its protected functional groups, which enable stepwise derivatization. Also utilized in

Used as a key chiral intermediate in the synthesis of active pharmaceutical ingredients, particularly in the development of central nervous system (CNS) drugs and antipsychotic medications. Its stereochemistry allows for selective interactions with biological targets, improving drug efficacy and reducing side effects. Commonly employed in medicinal chemistry for constructing complex piperazine-based structures due to its protected functional groups, which enable stepwise derivatization. Also utilized in the preparation of protease inhibitors and receptor agonists/antagonists in research settings.

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