(R)-tert-Butyl 3-oxo-2-phenylpiperazine-1-carboxylate

95%

Reagent Code: #37597
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CAS Number 2135284-21-6

science Other reagents with same CAS 2135284-21-6

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Weight 276.3309 g/mol
Formula C₁₅H₂₀N₂O₃
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MDL Number MFCD32173522
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description Product Description

This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various biologically active molecules. It plays a crucial role in the development of drugs targeting neurological disorders, particularly those involving serotonin and dopamine receptors. Its structural features make it valuable for designing compounds with potential antipsychotic or antidepressant properties. Additionally, it is employed in research settings for studying enzyme inhibition mechanisms and exploring new therapeutic pathways. Its chiral nature also makes it useful in asymmetric synthesis, contributing to the production of enantiomerically pure pharmaceuticals.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿15,318.00

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(R)-tert-Butyl 3-oxo-2-phenylpiperazine-1-carboxylate
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This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various biologically active molecules. It plays a crucial role in the development of drugs targeting neurological disorders, particularly those involving serotonin and dopamine receptors. Its structural features make it valuable for designing compounds with potential antipsychotic or antidepressant properties. Additionally, it is employed in research settings for studying enzyme inhibition mechanisms

This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various biologically active molecules. It plays a crucial role in the development of drugs targeting neurological disorders, particularly those involving serotonin and dopamine receptors. Its structural features make it valuable for designing compounds with potential antipsychotic or antidepressant properties. Additionally, it is employed in research settings for studying enzyme inhibition mechanisms and exploring new therapeutic pathways. Its chiral nature also makes it useful in asymmetric synthesis, contributing to the production of enantiomerically pure pharmaceuticals.

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