(R)-tert-Butyl 2,4-dibenzylpiperazine-1-carboxylate

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Reagent Code: #230846
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CAS Number 481038-74-8

science Other reagents with same CAS 481038-74-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 366.5 g/mol
Formula C₂₃H₃₀N₂O₂
badge Registry Numbers
MDL Number MFCD13248829
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules requiring stereochemical control. Its piperazine backbone with benzyl substituents makes it valuable in medicinal chemistry for constructing complex nitrogen-containing heterocycles. The tert-butyloxycarbonyl (Boc) group allows for selective protection during multi-step syntheses, enabling efficient route design in drug discovery. Commonly employed in the preparation of protease inhibitors and receptor modulators where the (R)-enantiomer imparts desired biological activity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿15,410.00
inventory 1g
10-20 days ฿26,090.00
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(R)-tert-Butyl 2,4-dibenzylpiperazine-1-carboxylate
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Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules requiring stereochemical control. Its piperazine backbone with benzyl substituents makes it valuable in medicinal chemistry for constructing complex nitrogen-containing heterocycles. The tert-butyloxycarbonyl (Boc) group allows for selective protection during multi-step syntheses, enabling efficient route design in drug discovery. Commonly employed in the preparation of prote

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules requiring stereochemical control. Its piperazine backbone with benzyl substituents makes it valuable in medicinal chemistry for constructing complex nitrogen-containing heterocycles. The tert-butyloxycarbonyl (Boc) group allows for selective protection during multi-step syntheses, enabling efficient route design in drug discovery. Commonly employed in the preparation of protease inhibitors and receptor modulators where the (R)-enantiomer imparts desired biological activity.

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