Di-tert-butyl (R)-2-(2-hydroxyethyl)piperazine-1,4-dicarboxylate

98%

Reagent Code: #229398
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CAS Number 2224423-03-2

science Other reagents with same CAS 2224423-03-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 330.42 g/mol
Formula C₁₆H₃₀N₂O₅
thermostat Physical Properties
Boiling Point 420.6±20.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.108±0.06 g/cm3(Predicted)
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 requiring stereochemical control. Its protected piperazine core with a hydroxyethyl side chain allows for selective functionalization in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and other therapeutic agents where the (R)-configuration plays a critical role in biological activity. The tert-butyl carbamate (Boc) groups provide stability during reactions and can be removed under mild acidic conditions, enabling further derivatization. Also utilized in medicinal chemistry for constructing drug candidates targeting central nervous system disorders and infectious diseases.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,480.00
inventory 250mg
10-20 days ฿14,420.00

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Di-tert-butyl (R)-2-(2-hydroxyethyl)piperazine-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 requiring stereochemical control. Its protected piperazine core with a hydroxyethyl side chain allows for selective functionalization in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and other therapeutic agents where the (R)-configuration plays a critical role in biological activity. The tert-butyl carbamate (Boc) groups provide stability

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules requiring stereochemical control. Its protected piperazine core with a hydroxyethyl side chain allows for selective functionalization in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and other therapeutic agents where the (R)-configuration plays a critical role in biological activity. The tert-butyl carbamate (Boc) groups provide stability during reactions and can be removed under mild acidic conditions, enabling further derivatization. Also utilized in medicinal chemistry for constructing drug candidates targeting central nervous system disorders and infectious diseases.

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