Dibenzyl (R)-2-methylpiperazine-1,4-dicarboxylate

98%

Reagent Code: #229472
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CAS Number 1047975-20-1

science Other reagents with same CAS 1047975-20-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 368.43 g/mol
Formula C₂₁H₂₄N₂O₄
thermostat Physical Properties
Boiling Point 507.7±45.0 °C(Predicted)
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates requiring stereochemical control. Its protected piperazine structure allows for selective functionalization, making it valuable in medicinal chemistry for creating protease inhibitors, receptor agonists, or antagonists. Commonly employed in asymmetric synthesis and solid-phase peptide synthesis due to its stability and defined stereochemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,400.00
inventory 250mg
10-20 days ฿5,780.00
inventory 1g
10-20 days ฿15,560.00
Dibenzyl (R)-2-methylpiperazine-1,4-dicarboxylate
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates requiring stereochemical control. Its protected piperazine structure allows for selective functionalization, making it valuable in medicinal chemistry for creating protease inhibitors, receptor agonists, or antagonists. Commonly employed in asymmetric synthesis and solid-phase peptide synthesis due to its stability and defined stereochemistry.

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates requiring stereochemical control. Its protected piperazine structure allows for selective functionalization, making it valuable in medicinal chemistry for creating protease inhibitors, receptor agonists, or antagonists. Commonly employed in asymmetric synthesis and solid-phase peptide synthesis due to its stability and defined stereochemistry.

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