(R)-tert-Butyl 2-benzylpiperazine-1-carboxylate

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Reagent Code: #230187
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CAS Number 947684-78-8

science Other reagents with same CAS 947684-78-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.37 g/mol
Formula C₁₆H₂₄N₂O₂
badge Registry Numbers
MDL Number MFCD07772094
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents and serotonin receptor modulators. Its piperazine backbone and stereochemistry make it valuable in optimizing drug selectivity and binding affinity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance metabolic stability and bioavailability in lead compounds. Also utilized in asymmetric synthesis where the (R)-enantiomer imparts specific biological activity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿434.50
inventory 1g
10-20 days ฿3,060.00
inventory 5g
10-20 days ฿10,990.00

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(R)-tert-Butyl 2-benzylpiperazine-1-carboxylate
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Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents and serotonin receptor modulators. Its piperazine backbone and stereochemistry make it valuable in optimizing drug selectivity and binding affinity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance metabolic stability and bioavailability in lead compounds. Also utilized in asymmetric synth

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents and serotonin receptor modulators. Its piperazine backbone and stereochemistry make it valuable in optimizing drug selectivity and binding affinity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance metabolic stability and bioavailability in lead compounds. Also utilized in asymmetric synthesis where the (R)-enantiomer imparts specific biological activity.

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