(3S,5S)-Benzyl 3,5-dimethylpiperazine-1-carboxylate

97%

Reagent Code: #232482
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CAS Number 874279-60-4

science Other reagents with same CAS 874279-60-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.32 g/mol
Formula C₁₄H₂₀N₂O₂
badge Registry Numbers
MDL Number MFCD27988069
thermostat Physical Properties
Boiling Point 364.6±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.071±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules targeting central nervous system disorders. Its piperazine scaffold is valuable for constructing drug candidates with enhanced binding affinity and selectivity. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the stereochemical control it offers. Also utilized in the preparation of protease inhibitors and receptor modulators, where the carbamate-protected amine allows for selective functionalization during multi-step syntheses.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿35,000.00
(3S,5S)-Benzyl 3,5-dimethylpiperazine-1-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules targeting central nervous system disorders. Its piperazine scaffold is valuable for constructing drug candidates with enhanced binding affinity and selectivity. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the stereochemical control it offers. Also utilized in the preparation of protease inhibitors and receptor modulators, where the ca

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules targeting central nervous system disorders. Its piperazine scaffold is valuable for constructing drug candidates with enhanced binding affinity and selectivity. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the stereochemical control it offers. Also utilized in the preparation of protease inhibitors and receptor modulators, where the carbamate-protected amine allows for selective functionalization during multi-step syntheses.

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