(R)-3-(tert-Butoxymethyl)piperazin-2-one

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Reagent Code: #228630
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CAS Number 1222102-49-9

science Other reagents with same CAS 1222102-49-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.25 g/mol
Formula C₉H₁₈N₂O₂
badge Registry Numbers
MDL Number MFCD28001875
thermostat Physical Properties
Boiling Point 330.0±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 0.987±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) drugs and antidiabetic medications. Its structural configuration supports the formation of bioactive molecules with high enantioselectivity, making it valuable in asymmetric synthesis. Commonly employed in the preparation of protease inhibitors and kinase inhibitors due to its ability to enhance metabolic stability and binding affinity. Also utilized in medicinal chemistry for constructing peptidomimetic frameworks, where the (R)-configuration contributes to improved pharmacokinetic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,220.00

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(R)-3-(tert-Butoxymethyl)piperazin-2-one
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) drugs and antidiabetic medications. Its structural configuration supports the formation of bioactive molecules with high enantioselectivity, making it valuable in asymmetric synthesis. Commonly employed in the preparation of protease inhibitors and kinase inhibitors due to its ability to enhance metabolic stability and binding affinity. Also utilized in medicinal chemi
Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) drugs and antidiabetic medications. Its structural configuration supports the formation of bioactive molecules with high enantioselectivity, making it valuable in asymmetric synthesis. Commonly employed in the preparation of protease inhibitors and kinase inhibitors due to its ability to enhance metabolic stability and binding affinity. Also utilized in medicinal chemistry for constructing peptidomimetic frameworks, where the (R)-configuration contributes to improved pharmacokinetic properties.
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